Canonical Allele Identifier: CA409103972
Gene: HNF4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44406208G>C , CM000682.2:g.44406208G>C GRCh38
NC_000020.10:g.43034848G>C , CM000682.1:g.43034848G>C GRCh37
NC_000020.9:g.42468262G>C NCBI36
NG_009818.1:g.55408G>C , LRG_483:g.55408G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.200G>C MANE Select ENSP00000315180.4:p.Arg67Pro
ENST00000316099.10:c.266G>C ENSP00000312987.3:p.Arg89Pro
ENST00000619550.5:c.240G>C
ENST00000681977.1:c.242G>C ENSP00000507189.1:p.Arg81Pro
ENST00000682169.1:c.219G>C
ENST00000683148.1:n.242G>C
ENST00000683657.1:n.242G>C
ENST00000684046.1:c.242G>C ENSP00000507555.1:p.Arg81Pro
ENST00000684136.1:c.242G>C ENSP00000507389.1:p.Arg81Pro
ENST00000684476.1:c.223G>C ENSP00000507529.1:p.Gly75Arg
ENST00000316099.9:c.266G>C ENSP00000312987.3:p.Arg89Pro
ENST00000316099.8:c.266G>C ENSP00000312987.3:p.Arg89Pro
ENST00000316673.8:c.200G>C ENSP00000315180.4:p.Arg67Pro
ENST00000372920.1:c.*33G>C ENSP00000362011.1:n.*33G>C
ENST00000415691.2:c.266G>C ENSP00000412111.1:p.Arg89Pro
ENST00000443598.6:c.266G>C ENSP00000410911.2:p.Arg89Pro
ENST00000457232.5:c.200G>C ENSP00000396216.1:p.Arg67Pro
ENST00000609262.5:c.191G>C ENSP00000476310.1:p.Arg64Pro
ENST00000609795.5:c.200G>C ENSP00000476609.1:p.Arg67Pro
ENST00000619550.4:c.191G>C ENSP00000481331.1:p.Arg64Pro
NM_000457.4:c.266G>C , LRG_483t2:c.266G>C NP_000448.3:p.Arg89Pro
NM_001030003.2:c.200G>C NP_001025174.1:p.Arg67Pro
NM_001030004.2:c.200G>C NP_001025175.1:p.Arg67Pro
NM_001258355.1:c.245G>C NP_001245284.1:p.Arg82Pro
NM_001287182.1:c.191G>C NP_001274111.1:p.Arg64Pro
NM_001287183.1:c.191G>C , LRG_483t3:c.191G>C NP_001274112.1:p.Arg64Pro
NM_001287184.1:c.191G>C NP_001274113.1:p.Arg64Pro
NM_175914.4:c.200G>C , LRG_483t1:c.200G>C NP_787110.2:p.Arg67Pro
NM_178849.2:c.266G>C NP_849180.1:p.Arg89Pro
NM_178850.2:c.266G>C NP_849181.1:p.Arg89Pro
XM_005260407.2:c.383G>C XP_005260464.1:p.Arg128Pro
XM_011528797.1:c.314G>C XP_011527099.1:p.Arg105Pro
XM_011528798.1:c.314G>C XP_011527100.1:p.Arg105Pro
XM_005260407.4:c.383G>C XP_005260464.1:p.Arg128Pro
NM_001030003.3:c.200G>C NP_001025174.1:p.Arg67Pro
NM_001030004.3:c.200G>C NP_001025175.1:p.Arg67Pro
NM_001258355.2:c.245G>C NP_001245284.1:p.Arg82Pro
NM_001287182.2:c.191G>C NP_001274111.1:p.Arg64Pro
NM_001287184.2:c.191G>C NP_001274113.1:p.Arg64Pro
NM_178849.3:c.266G>C NP_849180.1:p.Arg89Pro
NM_178850.3:c.266G>C NP_849181.1:p.Arg89Pro
NM_000457.5:c.266G>C NP_000448.3:p.Arg89Pro
NM_000457.6:c.266G>C NP_000448.3:p.Arg89Pro
NM_001287183.2:c.191G>C NP_001274112.1:p.Arg64Pro
NM_175914.5:c.200G>C MANE Select NP_787110.2:p.Arg67Pro