Canonical Allele Identifier: CA409105732
Gene: HNF4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413772T>C , CM000682.2:g.44413772T>C GRCh38
NC_000020.10:g.43042412T>C , CM000682.1:g.43042412T>C GRCh37
NC_000020.9:g.42475826T>C NCBI36
NG_009818.1:g.62972T>C , LRG_483:g.62972T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.398T>C MANE Select ENSP00000315180.4:p.Leu133Pro
ENST00000316099.10:c.464T>C ENSP00000312987.3:p.Leu155Pro
ENST00000619550.5:c.438T>C
ENST00000683148.1:n.440T>C
ENST00000683657.1:n.1588T>C
ENST00000316099.9:c.464T>C ENSP00000312987.3:p.Leu155Pro
ENST00000316099.8:c.464T>C ENSP00000312987.3:p.Leu155Pro
ENST00000316673.8:c.398T>C ENSP00000315180.4:p.Leu133Pro
ENST00000372920.1:c.*231T>C ENSP00000362011.1:n.*231T>C
ENST00000415691.2:c.464T>C ENSP00000412111.1:p.Leu155Pro
ENST00000443598.6:c.464T>C ENSP00000410911.2:p.Leu155Pro
ENST00000457232.5:c.398T>C ENSP00000396216.1:p.Leu133Pro
ENST00000609795.5:c.398T>C ENSP00000476609.1:p.Leu133Pro
ENST00000619550.4:c.389T>C ENSP00000481331.1:p.Leu130Pro
NM_000457.4:c.464T>C , LRG_483t2:c.464T>C NP_000448.3:p.Leu155Pro
NM_001030003.2:c.398T>C NP_001025174.1:p.Leu133Pro
NM_001030004.2:c.398T>C NP_001025175.1:p.Leu133Pro
NM_001258355.1:c.443T>C NP_001245284.1:p.Leu148Pro
NM_001287182.1:c.389T>C NP_001274111.1:p.Leu130Pro
NM_001287183.1:c.389T>C , LRG_483t3:c.389T>C NP_001274112.1:p.Leu130Pro
NM_001287184.1:c.389T>C NP_001274113.1:p.Leu130Pro
NM_175914.4:c.398T>C , LRG_483t1:c.398T>C NP_787110.2:p.Leu133Pro
NM_178849.2:c.464T>C NP_849180.1:p.Leu155Pro
NM_178850.2:c.464T>C NP_849181.1:p.Leu155Pro
XM_005260407.2:c.581T>C XP_005260464.1:p.Leu194Pro
XM_011528797.1:c.512T>C XP_011527099.1:p.Leu171Pro
XM_011528798.1:c.512T>C XP_011527100.1:p.Leu171Pro
XM_005260407.4:c.581T>C XP_005260464.1:p.Leu194Pro
NM_001030003.3:c.398T>C NP_001025174.1:p.Leu133Pro
NM_001030004.3:c.398T>C NP_001025175.1:p.Leu133Pro
NM_001258355.2:c.443T>C NP_001245284.1:p.Leu148Pro
NM_001287182.2:c.389T>C NP_001274111.1:p.Leu130Pro
NM_001287184.2:c.389T>C NP_001274113.1:p.Leu130Pro
NM_178849.3:c.464T>C NP_849180.1:p.Leu155Pro
NM_178850.3:c.464T>C NP_849181.1:p.Leu155Pro
NM_000457.5:c.464T>C NP_000448.3:p.Leu155Pro
NM_000457.6:c.464T>C NP_000448.3:p.Leu155Pro
NM_001287183.2:c.389T>C NP_001274112.1:p.Leu130Pro
NM_175914.5:c.398T>C MANE Select NP_787110.2:p.Leu133Pro