Canonical Allele Identifier: CA2005595573

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058768T= , CM000673.2:g.123058768T=	GRCh38
NC_000011.9:g.122929476T= , CM000673.1:g.122929476T=	GRCh37
NC_000011.8:g.122434686T=	NCBI36
NG_029473.1:g.8369A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1386A= MANE Select	ENSP00000432083.1:p.Thr462=
ENST00000227378.7:c.1386A=	ENSP00000227378.3:p.Thr462=
ENST00000453788.6:c.1386A=	ENSP00000404372.2:p.Thr462=
ENST00000524552.5:c.159A=	ENSP00000435908.1:p.Thr53=
ENST00000526110.5:c.1329A=	ENSP00000433584.1:p.Thr443=
ENST00000526686.1:c.42A=	ENSP00000435019.1:p.Thr14=
ENST00000532091.1:n.1361A=
ENST00000532636.5:c.1386A=	ENSP00000437125.1:p.Thr462=
ENST00000533540.5:c.948A=	ENSP00000437189.1:p.Thr316=
ENST00000534319.5:c.678A=	ENSP00000433316.1:p.Thr226=
ENST00000534624.5:c.1386A=	ENSP00000432083.1:p.Thr462=
NM_006597.5:c.1386A=	NP_006588.1:p.Thr462=
NM_153201.3:c.1386A=	NP_694881.1:p.Thr462=
XM_011542798.1:c.1386A=	XP_011541100.1:p.Thr462=
NM_006597.6:c.1386A= MANE Select	NP_006588.1:p.Thr462=
NM_153201.4:c.1386A=	NP_694881.1:p.Thr462=