Canonical Allele Identifier: CA409105806
Gene: HNF4A HGNC NCBI

Linked Data

gnomAD v4: 20-44413793-C-A
MyVariant Identifiers: chr20:g.43042433C>A (hg19) chr20:g.44413793C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413793C>A , CM000682.2:g.44413793C>A GRCh38
NC_000020.10:g.43042433C>A , CM000682.1:g.43042433C>A GRCh37
NC_000020.9:g.42475847C>A NCBI36
NG_009818.1:g.62993C>A , LRG_483:g.62993C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.419C>A MANE Select ENSP00000315180.4:p.Ser140Tyr
ENST00000316099.10:c.485C>A ENSP00000312987.3:p.Ser162Tyr
ENST00000619550.5:c.459C>A
ENST00000683148.1:n.461C>A
ENST00000683657.1:n.1609C>A
ENST00000316099.9:c.485C>A ENSP00000312987.3:p.Ser162Tyr
ENST00000316099.8:c.485C>A ENSP00000312987.3:p.Ser162Tyr
ENST00000316673.8:c.419C>A ENSP00000315180.4:p.Ser140Tyr
ENST00000372920.1:c.*252C>A ENSP00000362011.1:n.*252C>A
ENST00000415691.2:c.485C>A ENSP00000412111.1:p.Ser162Tyr
ENST00000443598.6:c.485C>A ENSP00000410911.2:p.Ser162Tyr
ENST00000457232.5:c.419C>A ENSP00000396216.1:p.Ser140Tyr
ENST00000609795.5:c.419C>A ENSP00000476609.1:p.Ser140Tyr
ENST00000619550.4:c.410C>A ENSP00000481331.1:p.Ser137Tyr
NM_000457.4:c.485C>A , LRG_483t2:c.485C>A NP_000448.3:p.Ser162Tyr
NM_001030003.2:c.419C>A NP_001025174.1:p.Ser140Tyr
NM_001030004.2:c.419C>A NP_001025175.1:p.Ser140Tyr
NM_001258355.1:c.464C>A NP_001245284.1:p.Ser155Tyr
NM_001287182.1:c.410C>A NP_001274111.1:p.Ser137Tyr
NM_001287183.1:c.410C>A , LRG_483t3:c.410C>A NP_001274112.1:p.Ser137Tyr
NM_001287184.1:c.410C>A NP_001274113.1:p.Ser137Tyr
NM_175914.4:c.419C>A , LRG_483t1:c.419C>A NP_787110.2:p.Ser140Tyr
NM_178849.2:c.485C>A NP_849180.1:p.Ser162Tyr
NM_178850.2:c.485C>A NP_849181.1:p.Ser162Tyr
XM_005260407.2:c.602C>A XP_005260464.1:p.Ser201Tyr
XM_011528797.1:c.533C>A XP_011527099.1:p.Ser178Tyr
XM_011528798.1:c.533C>A XP_011527100.1:p.Ser178Tyr
XM_005260407.4:c.602C>A XP_005260464.1:p.Ser201Tyr
NM_001030003.3:c.419C>A NP_001025174.1:p.Ser140Tyr
NM_001030004.3:c.419C>A NP_001025175.1:p.Ser140Tyr
NM_001258355.2:c.464C>A NP_001245284.1:p.Ser155Tyr
NM_001287182.2:c.410C>A NP_001274111.1:p.Ser137Tyr
NM_001287184.2:c.410C>A NP_001274113.1:p.Ser137Tyr
NM_178849.3:c.485C>A NP_849180.1:p.Ser162Tyr
NM_178850.3:c.485C>A NP_849181.1:p.Ser162Tyr
NM_000457.5:c.485C>A NP_000448.3:p.Ser162Tyr
NM_000457.6:c.485C>A NP_000448.3:p.Ser162Tyr
NM_001287183.2:c.410C>A NP_001274112.1:p.Ser137Tyr
NM_175914.5:c.419C>A MANE Select NP_787110.2:p.Ser140Tyr
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