Canonical Allele Identifier: CA2005597145

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059233G= , CM000673.2:g.123059233G=	GRCh38
NC_000011.9:g.122929941G= , CM000673.1:g.122929941G=	GRCh37
NC_000011.8:g.122435151G=	NCBI36
NG_029473.1:g.7904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1149C= MANE Select	ENSP00000432083.1:p.Asp383=
ENST00000227378.7:c.1149C=	ENSP00000227378.3:p.Asp383=
ENST00000453788.6:c.1149C=	ENSP00000404372.2:p.Asp383=
ENST00000524552.5:c.-79C=	ENSP00000435908.1:n.-79C=
ENST00000526110.5:c.1092C=	ENSP00000433584.1:p.Asp364=
ENST00000526862.1:n.427C=
ENST00000527983.5:n.1509C=
ENST00000532091.1:n.896C=
ENST00000532636.5:c.1149C=	ENSP00000437125.1:p.Asp383=
ENST00000533238.5:n.381-130C=
ENST00000533540.5:c.711C=	ENSP00000437189.1:p.Asp237=
ENST00000534319.5:c.441C=	ENSP00000433316.1:p.Asp147=
ENST00000534624.5:c.1149C=	ENSP00000432083.1:p.Asp383=
NM_006597.5:c.1149C=	NP_006588.1:p.Asp383=
NM_153201.3:c.1149C=	NP_694881.1:p.Asp383=
XM_011542798.1:c.1149C=	XP_011541100.1:p.Asp383=
NM_006597.6:c.1149C= MANE Select	NP_006588.1:p.Asp383=
NM_153201.4:c.1149C=	NP_694881.1:p.Asp383=