Canonical Allele Identifier: CA2005594632

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058441A= , CM000673.2:g.123058441A=	GRCh38
NC_000011.9:g.122929149A= , CM000673.1:g.122929149A=	GRCh37
NC_000011.8:g.122434359A=	NCBI36
NG_029473.1:g.8696T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1566T= MANE Select	ENSP00000432083.1:p.Ala522=
ENST00000227378.7:c.1566T=	ENSP00000227378.3:p.Ala522=
ENST00000453788.6:c.1387+326T=	ENSP00000404372.2:n.1387+326T=
ENST00000524552.5:c.339T=	ENSP00000435908.1:p.Ala113=
ENST00000526110.5:c.1509T=	ENSP00000433584.1:p.Ala503=
ENST00000526686.1:c.222T=	ENSP00000435019.1:p.Ala74=
ENST00000532091.1:n.1688T=
ENST00000532636.5:c.1566T=	ENSP00000437125.1:p.Ala522=
ENST00000533540.5:c.1128T=	ENSP00000437189.1:p.Ala376=
ENST00000534319.5:c.858T=	ENSP00000433316.1:p.Ala286=
ENST00000534624.5:c.1566T=	ENSP00000432083.1:p.Ala522=
NM_006597.5:c.1566T=	NP_006588.1:p.Ala522=
NM_153201.3:c.1387+326T=	NP_694881.1:n.1387+326T=
XM_011542798.1:c.1566T=	XP_011541100.1:p.Ala522=
NM_006597.6:c.1566T= MANE Select	NP_006588.1:p.Ala522=
NM_153201.4:c.1387+326T=	NP_694881.1:n.1387+326T=