Canonical Allele Identifier: CA409105446
Gene: HNF4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.43042352A>T (hg19) chr20:g.44413712A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413712A>T , CM000682.2:g.44413712A>T GRCh38
NC_000020.10:g.43042352A>T , CM000682.1:g.43042352A>T GRCh37
NC_000020.9:g.42475766A>T NCBI36
NG_009818.1:g.62912A>T , LRG_483:g.62912A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.338A>T MANE Select ENSP00000315180.4:p.Asp113Val
ENST00000316099.10:c.404A>T ENSP00000312987.3:p.Asp135Val
ENST00000619550.5:c.378A>T
ENST00000683148.1:n.380A>T
ENST00000683657.1:n.1528A>T
ENST00000316099.9:c.404A>T ENSP00000312987.3:p.Asp135Val
ENST00000316099.8:c.404A>T ENSP00000312987.3:p.Asp135Val
ENST00000316673.8:c.338A>T ENSP00000315180.4:p.Asp113Val
ENST00000372920.1:c.*171A>T ENSP00000362011.1:n.*171A>T
ENST00000415691.2:c.404A>T ENSP00000412111.1:p.Asp135Val
ENST00000443598.6:c.404A>T ENSP00000410911.2:p.Asp135Val
ENST00000457232.5:c.338A>T ENSP00000396216.1:p.Asp113Val
ENST00000609795.5:c.338A>T ENSP00000476609.1:p.Asp113Val
ENST00000619550.4:c.329A>T ENSP00000481331.1:p.Asp110Val
NM_000457.4:c.404A>T , LRG_483t2:c.404A>T NP_000448.3:p.Asp135Val
NM_001030003.2:c.338A>T NP_001025174.1:p.Asp113Val
NM_001030004.2:c.338A>T NP_001025175.1:p.Asp113Val
NM_001258355.1:c.383A>T NP_001245284.1:p.Asp128Val
NM_001287182.1:c.329A>T NP_001274111.1:p.Asp110Val
NM_001287183.1:c.329A>T , LRG_483t3:c.329A>T NP_001274112.1:p.Asp110Val
NM_001287184.1:c.329A>T NP_001274113.1:p.Asp110Val
NM_175914.4:c.338A>T , LRG_483t1:c.338A>T NP_787110.2:p.Asp113Val
NM_178849.2:c.404A>T NP_849180.1:p.Asp135Val
NM_178850.2:c.404A>T NP_849181.1:p.Asp135Val
XM_005260407.2:c.521A>T XP_005260464.1:p.Asp174Val
XM_011528797.1:c.452A>T XP_011527099.1:p.Asp151Val
XM_011528798.1:c.452A>T XP_011527100.1:p.Asp151Val
XM_005260407.4:c.521A>T XP_005260464.1:p.Asp174Val
NM_001030003.3:c.338A>T NP_001025174.1:p.Asp113Val
NM_001030004.3:c.338A>T NP_001025175.1:p.Asp113Val
NM_001258355.2:c.383A>T NP_001245284.1:p.Asp128Val
NM_001287182.2:c.329A>T NP_001274111.1:p.Asp110Val
NM_001287184.2:c.329A>T NP_001274113.1:p.Asp110Val
NM_178849.3:c.404A>T NP_849180.1:p.Asp135Val
NM_178850.3:c.404A>T NP_849181.1:p.Asp135Val
NM_000457.5:c.404A>T NP_000448.3:p.Asp135Val
NM_000457.6:c.404A>T NP_000448.3:p.Asp135Val
NM_001287183.2:c.329A>T NP_001274112.1:p.Asp110Val
NM_175914.5:c.338A>T MANE Select NP_787110.2:p.Asp113Val
Search 100 bp 5'
Search 100 bp 3'