Canonical Allele Identifier: CA2005597085

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059215T= , CM000673.2:g.123059215T=	GRCh38
NC_000011.9:g.122929923T= , CM000673.1:g.122929923T=	GRCh37
NC_000011.8:g.122435133T=	NCBI36
NG_029473.1:g.7922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1167A= MANE Select	ENSP00000432083.1:p.Gln389=
ENST00000227378.7:c.1167A=	ENSP00000227378.3:p.Gln389=
ENST00000453788.6:c.1167A=	ENSP00000404372.2:p.Gln389=
ENST00000524552.5:c.-61A=	ENSP00000435908.1:n.-61A=
ENST00000526110.5:c.1110A=	ENSP00000433584.1:p.Gln370=
ENST00000526862.1:n.445A=
ENST00000532091.1:n.914A=
ENST00000532636.5:c.1167A=	ENSP00000437125.1:p.Gln389=
ENST00000533238.5:n.381-112A=
ENST00000533540.5:c.729A=	ENSP00000437189.1:p.Gln243=
ENST00000534319.5:c.459A=	ENSP00000433316.1:p.Gln153=
ENST00000534624.5:c.1167A=	ENSP00000432083.1:p.Gln389=
NM_006597.5:c.1167A=	NP_006588.1:p.Gln389=
NM_153201.3:c.1167A=	NP_694881.1:p.Gln389=
XM_011542798.1:c.1167A=	XP_011541100.1:p.Gln389=
NM_006597.6:c.1167A= MANE Select	NP_006588.1:p.Gln389=
NM_153201.4:c.1167A=	NP_694881.1:p.Gln389=