Canonical Allele Identifier: CA645608981

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44406134_44406135delinsAA , CM000682.2:g.44406134_44406135delinsAA	GRCh38
NC_000020.10:g.43034774_43034775delinsAA , CM000682.1:g.43034774_43034775delinsAA	GRCh37
NC_000020.9:g.42468188_42468189delinsAA	NCBI36
NG_009818.1:g.55334_55335delinsAA , LRG_483:g.55334_55335delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.126_127delinsAA MANE Select	ENSP00000315180.4:p.Asp43Asn
ENST00000316099.10:c.192_193delinsAA	ENSP00000312987.3:p.Asp65Asn
ENST00000619550.5:c.166_167delinsAA
ENST00000681977.1:c.168_169delinsAA	ENSP00000507189.1:p.Asp57Asn
ENST00000682169.1:c.145_146delinsAA
ENST00000683148.1:n.168_169delinsAA
ENST00000683657.1:n.168_169delinsAA
ENST00000684046.1:c.168_169delinsAA	ENSP00000507555.1:p.Asp57Asn
ENST00000684136.1:c.168_169delinsAA	ENSP00000507389.1:p.Asp57Asn
ENST00000684476.1:c.149_150delinsAA	ENSP00000507529.1:p.Gly50Glu
ENST00000316099.9:c.192_193delinsAA	ENSP00000312987.3:p.Asp65Asn
ENST00000316099.8:c.192_193delinsAA	ENSP00000312987.3:p.Asp65Asn
ENST00000316673.8:c.126_127delinsAA	ENSP00000315180.4:p.Asp43Asn
ENST00000372920.1:c.283_284delinsAA	ENSP00000362011.1:p.Gly95Lys
ENST00000415691.2:c.192_193delinsAA	ENSP00000412111.1:p.Asp65Asn
ENST00000443598.6:c.192_193delinsAA	ENSP00000410911.2:p.Asp65Asn
ENST00000457232.5:c.126_127delinsAA	ENSP00000396216.1:p.Asp43Asn
ENST00000609262.5:c.117_118delinsAA	ENSP00000476310.1:p.Asp40Asn
ENST00000609795.5:c.126_127delinsAA	ENSP00000476609.1:p.Asp43Asn
ENST00000619550.4:c.117_118delinsAA	ENSP00000481331.1:p.Asp40Asn
NM_000457.4:c.192_193delinsAA , LRG_483t2:c.192_193delinsAA	NP_000448.3:p.Asp65Asn
NM_001030003.2:c.126_127delinsAA	NP_001025174.1:p.Asp43Asn
NM_001030004.2:c.126_127delinsAA	NP_001025175.1:p.Asp43Asn
NM_001258355.1:c.171_172delinsAA	NP_001245284.1:p.Asp58Asn
NM_001287182.1:c.117_118delinsAA	NP_001274111.1:p.Asp40Asn
NM_001287183.1:c.117_118delinsAA , LRG_483t3:c.117_118delinsAA	NP_001274112.1:p.Asp40Asn
NM_001287184.1:c.117_118delinsAA	NP_001274113.1:p.Asp40Asn
NM_175914.4:c.126_127delinsAA , LRG_483t1:c.126_127delinsAA	NP_787110.2:p.Asp43Asn
NM_178849.2:c.192_193delinsAA	NP_849180.1:p.Asp65Asn
NM_178850.2:c.192_193delinsAA	NP_849181.1:p.Asp65Asn
XM_005260407.2:c.309_310delinsAA	XP_005260464.1:p.Asp104Asn
XM_011528797.1:c.240_241delinsAA	XP_011527099.1:p.Asp81Asn
XM_011528798.1:c.240_241delinsAA	XP_011527100.1:p.Asp81Asn
XM_005260407.4:c.309_310delinsAA	XP_005260464.1:p.Asp104Asn
NM_001030003.3:c.126_127delinsAA	NP_001025174.1:p.Asp43Asn
NM_001030004.3:c.126_127delinsAA	NP_001025175.1:p.Asp43Asn
NM_001258355.2:c.171_172delinsAA	NP_001245284.1:p.Asp58Asn
NM_001287182.2:c.117_118delinsAA	NP_001274111.1:p.Asp40Asn
NM_001287184.2:c.117_118delinsAA	NP_001274113.1:p.Asp40Asn
NM_178849.3:c.192_193delinsAA	NP_849180.1:p.Asp65Asn
NM_178850.3:c.192_193delinsAA	NP_849181.1:p.Asp65Asn
NM_000457.5:c.192_193delinsAA	NP_000448.3:p.Asp65Asn
NM_000457.6:c.192_193delinsAA	NP_000448.3:p.Asp65Asn
NM_001287183.2:c.117_118delinsAA	NP_001274112.1:p.Asp40Asn
NM_175914.5:c.126_127delinsAA MANE Select	NP_787110.2:p.Asp43Asn