Canonical Allele Identifier: CA409105829
Gene: HNF4A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.425A>G MANE Select ENSP00000315180.4:p.Gln142Arg
ENST00000316099.10:c.491A>G ENSP00000312987.3:p.Gln164Arg
ENST00000619550.5:c.465A>G
ENST00000683148.1:n.467A>G
ENST00000683657.1:n.1615A>G
ENST00000316099.9:c.491A>G ENSP00000312987.3:p.Gln164Arg
ENST00000316099.8:c.491A>G ENSP00000312987.3:p.Gln164Arg
ENST00000316673.8:c.425A>G ENSP00000315180.4:p.Gln142Arg
ENST00000372920.1:c.*258A>G ENSP00000362011.1:n.*258A>G
ENST00000415691.2:c.491A>G ENSP00000412111.1:p.Gln164Arg
ENST00000443598.6:c.491A>G ENSP00000410911.2:p.Gln164Arg
ENST00000457232.5:c.425A>G ENSP00000396216.1:p.Gln142Arg
ENST00000609795.5:c.425A>G ENSP00000476609.1:p.Gln142Arg
ENST00000619550.4:c.416A>G ENSP00000481331.1:p.Gln139Arg
NM_000457.4:c.491A>G , LRG_483t2:c.491A>G NP_000448.3:p.Gln164Arg
NM_001030003.2:c.425A>G NP_001025174.1:p.Gln142Arg
NM_001030004.2:c.425A>G NP_001025175.1:p.Gln142Arg
NM_001258355.1:c.470A>G NP_001245284.1:p.Gln157Arg
NM_001287182.1:c.416A>G NP_001274111.1:p.Gln139Arg
NM_001287183.1:c.416A>G , LRG_483t3:c.416A>G NP_001274112.1:p.Gln139Arg
NM_001287184.1:c.416A>G NP_001274113.1:p.Gln139Arg
NM_175914.4:c.425A>G , LRG_483t1:c.425A>G NP_787110.2:p.Gln142Arg
NM_178849.2:c.491A>G NP_849180.1:p.Gln164Arg
NM_178850.2:c.491A>G NP_849181.1:p.Gln164Arg
XM_005260407.2:c.608A>G XP_005260464.1:p.Gln203Arg
XM_011528797.1:c.539A>G XP_011527099.1:p.Gln180Arg
XM_011528798.1:c.539A>G XP_011527100.1:p.Gln180Arg
XM_005260407.4:c.608A>G XP_005260464.1:p.Gln203Arg
NM_001030003.3:c.425A>G NP_001025174.1:p.Gln142Arg
NM_001030004.3:c.425A>G NP_001025175.1:p.Gln142Arg
NM_001258355.2:c.470A>G NP_001245284.1:p.Gln157Arg
NM_001287182.2:c.416A>G NP_001274111.1:p.Gln139Arg
NM_001287184.2:c.416A>G NP_001274113.1:p.Gln139Arg
NM_178849.3:c.491A>G NP_849180.1:p.Gln164Arg
NM_178850.3:c.491A>G NP_849181.1:p.Gln164Arg
NM_000457.5:c.491A>G NP_000448.3:p.Gln164Arg
NM_000457.6:c.491A>G NP_000448.3:p.Gln164Arg
NM_001287183.2:c.416A>G NP_001274112.1:p.Gln139Arg
NM_175914.5:c.425A>G MANE Select NP_787110.2:p.Gln142Arg