Canonical Allele Identifier: CA2005597059

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059203G= , CM000673.2:g.123059203G=	GRCh38
NC_000011.9:g.122929911G= , CM000673.1:g.122929911G=	GRCh37
NC_000011.8:g.122435121G=	NCBI36
NG_029473.1:g.7934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1179C= MANE Select	ENSP00000432083.1:p.Leu393=
ENST00000227378.7:c.1179C=	ENSP00000227378.3:p.Leu393=
ENST00000453788.6:c.1179C=	ENSP00000404372.2:p.Leu393=
ENST00000524552.5:c.-49C=	ENSP00000435908.1:n.-49C=
ENST00000526110.5:c.1122C=	ENSP00000433584.1:p.Leu374=
ENST00000526862.1:n.457C=
ENST00000532091.1:n.926C=
ENST00000532636.5:c.1179C=	ENSP00000437125.1:p.Leu393=
ENST00000533238.5:n.381-100C=
ENST00000533540.5:c.741C=	ENSP00000437189.1:p.Leu247=
ENST00000534319.5:c.471C=	ENSP00000433316.1:p.Leu157=
ENST00000534624.5:c.1179C=	ENSP00000432083.1:p.Leu393=
NM_006597.5:c.1179C=	NP_006588.1:p.Leu393=
NM_153201.3:c.1179C=	NP_694881.1:p.Leu393=
XM_011542798.1:c.1179C=	XP_011541100.1:p.Leu393=
NM_006597.6:c.1179C= MANE Select	NP_006588.1:p.Leu393=
NM_153201.4:c.1179C=	NP_694881.1:p.Leu393=