Canonical Allele Identifier: CA2005596977

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059180A= , CM000673.2:g.123059180A=	GRCh38
NC_000011.9:g.122929888A= , CM000673.1:g.122929888A=	GRCh37
NC_000011.8:g.122435098A=	NCBI36
NG_029473.1:g.7957T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1202T= MANE Select	ENSP00000432083.1:p.Leu401=
ENST00000227378.7:c.1202T=	ENSP00000227378.3:p.Leu401=
ENST00000453788.6:c.1202T=	ENSP00000404372.2:p.Leu401=
ENST00000524552.5:c.-26T=	ENSP00000435908.1:n.-26T=
ENST00000526110.5:c.1145T=	ENSP00000433584.1:p.Leu382=
ENST00000526862.1:n.480T=
ENST00000532091.1:n.949T=
ENST00000532636.5:c.1202T=	ENSP00000437125.1:p.Leu401=
ENST00000533238.5:n.381-77T=
ENST00000533540.5:c.764T=	ENSP00000437189.1:p.Leu255=
ENST00000534319.5:c.494T=	ENSP00000433316.1:p.Leu165=
ENST00000534624.5:c.1202T=	ENSP00000432083.1:p.Leu401=
NM_006597.5:c.1202T=	NP_006588.1:p.Leu401=
NM_153201.3:c.1202T=	NP_694881.1:p.Leu401=
XM_011542798.1:c.1202T=	XP_011541100.1:p.Leu401=
NM_006597.6:c.1202T= MANE Select	NP_006588.1:p.Leu401=
NM_153201.4:c.1202T=	NP_694881.1:p.Leu401=