Canonical Allele Identifier: CA2260155218

Gene: HAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727107T= , CM000679.2:g.41727107T=	GRCh38
NC_000017.10:g.39883359T= , CM000679.1:g.39883359T=	GRCh37
NC_000017.9:g.37136885T=	NCBI36
NG_009090.2:g.64606A= , LRG_401:g.64606A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1313A= MANE Select	ENSP00000334002.4:p.Glu438=
ENST00000310778.5:c.1469A=	ENSP00000309392.5:p.Glu490=
ENST00000341193.9:c.1262A=	ENSP00000343170.5:p.Glu421=
ENST00000347901.8:c.1313A=	ENSP00000334002.4:p.Glu438=
ENST00000393939.6:c.1238A=	ENSP00000377513.2:p.Glu413=
NM_001079870.1:c.1262A=	NP_001073339.1:p.Glu421=
NM_001079871.1:c.1238A=	NP_001073340.1:p.Glu413=
NM_177977.2:c.1313A=	NP_817084.2:p.Glu438=
NM_001367459.1:c.1409A=	NP_001354388.1:p.Glu470=
NM_001367460.1:c.1373A=	NP_001354389.1:p.Glu458=
NM_001367461.1:c.1238A=	NP_001354390.1:p.Glu413=
NM_001367462.1:c.1238A=	NP_001354391.1:p.Glu413=
NM_177977.3:c.1313A= MANE Select	NP_817084.2:p.Glu438=