Canonical Allele Identifier: CA409105831
Gene: HNF4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413799A>T , CM000682.2:g.44413799A>T GRCh38
NC_000020.10:g.43042439A>T , CM000682.1:g.43042439A>T GRCh37
NC_000020.9:g.42475853A>T NCBI36
NG_009818.1:g.62999A>T , LRG_483:g.62999A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.425A>T MANE Select ENSP00000315180.4:p.Gln142Leu
ENST00000316099.10:c.491A>T ENSP00000312987.3:p.Gln164Leu
ENST00000619550.5:c.465A>T
ENST00000683148.1:n.467A>T
ENST00000683657.1:n.1615A>T
ENST00000316099.9:c.491A>T ENSP00000312987.3:p.Gln164Leu
ENST00000316099.8:c.491A>T ENSP00000312987.3:p.Gln164Leu
ENST00000316673.8:c.425A>T ENSP00000315180.4:p.Gln142Leu
ENST00000372920.1:c.*258A>T ENSP00000362011.1:n.*258A>T
ENST00000415691.2:c.491A>T ENSP00000412111.1:p.Gln164Leu
ENST00000443598.6:c.491A>T ENSP00000410911.2:p.Gln164Leu
ENST00000457232.5:c.425A>T ENSP00000396216.1:p.Gln142Leu
ENST00000609795.5:c.425A>T ENSP00000476609.1:p.Gln142Leu
ENST00000619550.4:c.416A>T ENSP00000481331.1:p.Gln139Leu
NM_000457.4:c.491A>T , LRG_483t2:c.491A>T NP_000448.3:p.Gln164Leu
NM_001030003.2:c.425A>T NP_001025174.1:p.Gln142Leu
NM_001030004.2:c.425A>T NP_001025175.1:p.Gln142Leu
NM_001258355.1:c.470A>T NP_001245284.1:p.Gln157Leu
NM_001287182.1:c.416A>T NP_001274111.1:p.Gln139Leu
NM_001287183.1:c.416A>T , LRG_483t3:c.416A>T NP_001274112.1:p.Gln139Leu
NM_001287184.1:c.416A>T NP_001274113.1:p.Gln139Leu
NM_175914.4:c.425A>T , LRG_483t1:c.425A>T NP_787110.2:p.Gln142Leu
NM_178849.2:c.491A>T NP_849180.1:p.Gln164Leu
NM_178850.2:c.491A>T NP_849181.1:p.Gln164Leu
XM_005260407.2:c.608A>T XP_005260464.1:p.Gln203Leu
XM_011528797.1:c.539A>T XP_011527099.1:p.Gln180Leu
XM_011528798.1:c.539A>T XP_011527100.1:p.Gln180Leu
XM_005260407.4:c.608A>T XP_005260464.1:p.Gln203Leu
NM_001030003.3:c.425A>T NP_001025174.1:p.Gln142Leu
NM_001030004.3:c.425A>T NP_001025175.1:p.Gln142Leu
NM_001258355.2:c.470A>T NP_001245284.1:p.Gln157Leu
NM_001287182.2:c.416A>T NP_001274111.1:p.Gln139Leu
NM_001287184.2:c.416A>T NP_001274113.1:p.Gln139Leu
NM_178849.3:c.491A>T NP_849180.1:p.Gln164Leu
NM_178850.3:c.491A>T NP_849181.1:p.Gln164Leu
NM_000457.5:c.491A>T NP_000448.3:p.Gln164Leu
NM_000457.6:c.491A>T NP_000448.3:p.Gln164Leu
NM_001287183.2:c.416A>T NP_001274112.1:p.Gln139Leu
NM_175914.5:c.425A>T MANE Select NP_787110.2:p.Gln142Leu