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NR_165391.1 - -
NR_165390.1 - -
NM_001378041.1 - NP_001364970.1
NM_001378043.1 - NP_001364972.1
NM_001378050.1 - NP_001364979.1
NM_012153.6 - NP_036285.2 (MANE)
NM_001378049.1 - NP_001364978.1
NM_001206615.2 - NP_001193544.1
NM_001378054.1 - NP_001364983.1
NM_001378042.1 - NP_001364971.1
NM_001378053.1 - NP_001364982.1
NM_001378055.1 - NP_001364984.1
NM_001378056.1 - NP_001364985.1
NM_001378044.1 - NP_001364973.1
NM_001378045.1 - NP_001364974.1
NM_001378051.1 - NP_001364980.1
NM_001378047.1 - NP_001364976.1
NM_001378048.1 - NP_001364977.1
NM_001206616.2 - NP_001193545.1
NM_001378052.1 - NP_001364981.1
NM_001378046.1 - NP_001364975.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
11
Location
Chr11:34,620,593-34,663,788
LOEUF
0.425
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ClinVar
Pathogenic/ Likely pa...
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VUS
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GnomAD
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Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
26298
Ensembl
ENSG00000135373
GeneCards
EHF
UniProt
Q9NZC4
KEGG
hsa:26298
gnomAD
ENSG00000135373
ICGC
ENSG00000135373
RefDIC
26298
RefEx
26298
DTX
EHF
AS-ALPS
EHF
EHF
ETS homologous factor
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