Canonical Allele Identifier: CA2005594708

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058465G= , CM000673.2:g.123058465G=	GRCh38
NC_000011.9:g.122929173G= , CM000673.1:g.122929173G=	GRCh37
NC_000011.8:g.122434383G=	NCBI36
NG_029473.1:g.8672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1542C= MANE Select	ENSP00000432083.1:p.Asp514=
ENST00000227378.7:c.1542C=	ENSP00000227378.3:p.Asp514=
ENST00000453788.6:c.1387+302C=	ENSP00000404372.2:n.1387+302C=
ENST00000524552.5:c.315C=	ENSP00000435908.1:p.Asp105=
ENST00000526110.5:c.1485C=	ENSP00000433584.1:p.Asp495=
ENST00000526686.1:c.198C=	ENSP00000435019.1:p.Asp66=
ENST00000532091.1:n.1664C=
ENST00000532636.5:c.1542C=	ENSP00000437125.1:p.Asp514=
ENST00000533540.5:c.1104C=	ENSP00000437189.1:p.Asp368=
ENST00000534319.5:c.834C=	ENSP00000433316.1:p.Asp278=
ENST00000534624.5:c.1542C=	ENSP00000432083.1:p.Asp514=
NM_006597.5:c.1542C=	NP_006588.1:p.Asp514=
NM_153201.3:c.1387+302C=	NP_694881.1:n.1387+302C=
XM_011542798.1:c.1542C=	XP_011541100.1:p.Asp514=
NM_006597.6:c.1542C= MANE Select	NP_006588.1:p.Asp514=
NM_153201.4:c.1387+302C=	NP_694881.1:n.1387+302C=