Canonical Allele Identifier: CA2005597182

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059251T= , CM000673.2:g.123059251T=	GRCh38
NC_000011.9:g.122929959T= , CM000673.1:g.122929959T=	GRCh37
NC_000011.8:g.122435169T=	NCBI36
NG_029473.1:g.7886A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1131A= MANE Select	ENSP00000432083.1:p.Ala377=
ENST00000227378.7:c.1131A=	ENSP00000227378.3:p.Ala377=
ENST00000453788.6:c.1131A=	ENSP00000404372.2:p.Ala377=
ENST00000524552.5:c.-97A=	ENSP00000435908.1:n.-97A=
ENST00000526110.5:c.1074A=	ENSP00000433584.1:p.Ala358=
ENST00000526862.1:n.409A=
ENST00000527983.5:n.1491A=
ENST00000532091.1:n.878A=
ENST00000532636.5:c.1131A=	ENSP00000437125.1:p.Ala377=
ENST00000533238.5:n.381-148A=
ENST00000533540.5:c.693A=	ENSP00000437189.1:p.Ala231=
ENST00000534319.5:c.423A=	ENSP00000433316.1:p.Ala141=
ENST00000534624.5:c.1131A=	ENSP00000432083.1:p.Ala377=
NM_006597.5:c.1131A=	NP_006588.1:p.Ala377=
NM_153201.3:c.1131A=	NP_694881.1:p.Ala377=
XM_011542798.1:c.1131A=	XP_011541100.1:p.Ala377=
NM_006597.6:c.1131A= MANE Select	NP_006588.1:p.Ala377=
NM_153201.4:c.1131A=	NP_694881.1:p.Ala377=