Canonical Allele Identifier: CA2260155229

Gene: HAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727135G= , CM000679.2:g.41727135G=	GRCh38
NC_000017.10:g.39883387G= , CM000679.1:g.39883387G=	GRCh37
NC_000017.9:g.37136913G=	NCBI36
NG_009090.2:g.64578C= , LRG_401:g.64578C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1285C= MANE Select	ENSP00000334002.4:p.Pro429=
ENST00000310778.5:c.1441C=	ENSP00000309392.5:p.Pro481=
ENST00000341193.9:c.1234C=	ENSP00000343170.5:p.Pro412=
ENST00000347901.8:c.1285C=	ENSP00000334002.4:p.Pro429=
ENST00000393939.6:c.1210C=	ENSP00000377513.2:p.Pro404=
NM_001079870.1:c.1234C=	NP_001073339.1:p.Pro412=
NM_001079871.1:c.1210C=	NP_001073340.1:p.Pro404=
NM_177977.2:c.1285C=	NP_817084.2:p.Pro429=
NM_001367459.1:c.1381C=	NP_001354388.1:p.Pro461=
NM_001367460.1:c.1345C=	NP_001354389.1:p.Pro449=
NM_001367461.1:c.1210C=	NP_001354390.1:p.Pro404=
NM_001367462.1:c.1210C=	NP_001354391.1:p.Pro404=
NM_177977.3:c.1285C= MANE Select	NP_817084.2:p.Pro429=