Canonical Allele Identifier: CA409106752
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 447518
dbSNP Id: rs1555816279

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44418432T>C , CM000682.2:g.44418432T>C GRCh38
NC_000020.10:g.43047072T>C , CM000682.1:g.43047072T>C GRCh37
NC_000020.9:g.42480486T>C NCBI36
NG_009818.1:g.67632T>C , LRG_483:g.67632T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.590T>C MANE Select ENSP00000315180.4:p.Leu197Pro
ENST00000316099.10:c.656T>C ENSP00000312987.3:p.Leu219Pro
ENST00000619550.5:c.630T>C
ENST00000683148.1:n.632T>C
ENST00000683657.1:n.1780T>C
ENST00000316099.9:c.656T>C ENSP00000312987.3:p.Leu219Pro
ENST00000316099.8:c.656T>C ENSP00000312987.3:p.Leu219Pro
ENST00000316673.8:c.590T>C ENSP00000315180.4:p.Leu197Pro
ENST00000372920.1:c.*423T>C ENSP00000362011.1:n.*423T>C
ENST00000415691.2:c.656T>C ENSP00000412111.1:p.Leu219Pro
ENST00000443598.6:c.656T>C ENSP00000410911.2:p.Leu219Pro
ENST00000457232.5:c.590T>C ENSP00000396216.1:p.Leu197Pro
ENST00000609795.5:c.590T>C ENSP00000476609.1:p.Leu197Pro
ENST00000619550.4:c.581T>C ENSP00000481331.1:p.Leu194Pro
NM_000457.4:c.656T>C , LRG_483t2:c.656T>C NP_000448.3:p.Leu219Pro
NM_001030003.2:c.590T>C NP_001025174.1:p.Leu197Pro
NM_001030004.2:c.590T>C NP_001025175.1:p.Leu197Pro
NM_001258355.1:c.635T>C NP_001245284.1:p.Leu212Pro
NM_001287182.1:c.581T>C NP_001274111.1:p.Leu194Pro
NM_001287183.1:c.581T>C , LRG_483t3:c.581T>C NP_001274112.1:p.Leu194Pro
NM_001287184.1:c.581T>C NP_001274113.1:p.Leu194Pro
NM_175914.4:c.590T>C , LRG_483t1:c.590T>C NP_787110.2:p.Leu197Pro
NM_178849.2:c.656T>C NP_849180.1:p.Leu219Pro
NM_178850.2:c.656T>C NP_849181.1:p.Leu219Pro
XM_005260407.2:c.773T>C XP_005260464.1:p.Leu258Pro
XM_011528797.1:c.704T>C XP_011527099.1:p.Leu235Pro
XM_011528798.1:c.704T>C XP_011527100.1:p.Leu235Pro
XM_005260407.4:c.773T>C XP_005260464.1:p.Leu258Pro
NM_001030003.3:c.590T>C NP_001025174.1:p.Leu197Pro
NM_001030004.3:c.590T>C NP_001025175.1:p.Leu197Pro
NM_001258355.2:c.635T>C NP_001245284.1:p.Leu212Pro
NM_001287182.2:c.581T>C NP_001274111.1:p.Leu194Pro
NM_001287184.2:c.581T>C NP_001274113.1:p.Leu194Pro
NM_178849.3:c.656T>C NP_849180.1:p.Leu219Pro
NM_178850.3:c.656T>C NP_849181.1:p.Leu219Pro
NM_000457.5:c.656T>C NP_000448.3:p.Leu219Pro
NM_000457.6:c.656T>C NP_000448.3:p.Leu219Pro
NM_001287183.2:c.581T>C NP_001274112.1:p.Leu194Pro
NM_175914.5:c.590T>C MANE Select NP_787110.2:p.Leu197Pro