Canonical Allele Identifier: CA14788710
Gene: HNF4A HGNC NCBI
HNF4A-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44361074T>C , CM000682.2:g.44361074T>C GRCh38
NC_000020.10:g.42989714T>C , CM000682.1:g.42989714T>C GRCh37
NC_000020.9:g.42423128T>C NCBI36
NG_009818.1:g.10274T>C , LRG_483:g.10274T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.49+5221T>C (HNF4A) MANE Select ENSP00000315180.4:n.49+5221T>C
ENST00000316673.8:c.49+5221T>C (HNF4A) ENSP00000315180.4:n.49+5221T>C
ENST00000457232.5:c.49+5221T>C (HNF4A) ENSP00000396216.1:n.49+5221T>C
ENST00000609262.5:c.-183+5221T>C (HNF4A) ENSP00000476310.1:n.-183+5221T>C
ENST00000609795.5:c.49+5221T>C (HNF4A) ENSP00000476609.1:n.49+5221T>C
ENST00000619550.4:c.-183+5221T>C (HNF4A) ENSP00000481331.1:n.-183+5221T>C
NM_001030003.2:c.49+5221T>C (HNF4A) NP_001025174.1:n.49+5221T>C
NM_001030004.2:c.49+5221T>C (HNF4A) NP_001025175.1:n.49+5221T>C
NM_001287182.1:c.-183+5221T>C (HNF4A) NP_001274111.1:n.-183+5221T>C
NM_001287183.1:c.-183+5221T>C , LRG_483t3:c.-183+5221T>C (HNF4A) NP_001274112.1:n.-183+5221T>C
NM_001287184.1:c.-183+5221T>C (HNF4A) NP_001274113.1:n.-183+5221T>C
NM_175914.4:c.49+5221T>C , LRG_483t1:c.49+5221T>C (HNF4A) NP_787110.2:n.49+5221T>C
NM_001030003.3:c.49+5221T>C (HNF4A) NP_001025174.1:n.49+5221T>C
NM_001030004.3:c.49+5221T>C (HNF4A) NP_001025175.1:n.49+5221T>C
NM_001287182.2:c.-183+5221T>C (HNF4A) NP_001274111.1:n.-183+5221T>C
NM_001287184.2:c.-183+5221T>C (HNF4A) NP_001274113.1:n.-183+5221T>C
NM_001287183.2:c.-183+5221T>C (HNF4A) NP_001274112.1:n.-183+5221T>C
NM_175914.5:c.49+5221T>C (HNF4A) MANE Select NP_787110.2:n.49+5221T>C
NR_172878.1:n.361-153A>G (HNF4A-AS1)
Search 100 bp 5'
Search 100 bp 3'