Canonical Allele Identifier: CA2005595645

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058801C= , CM000673.2:g.123058801C=	GRCh38
NC_000011.9:g.122929509C= , CM000673.1:g.122929509C=	GRCh37
NC_000011.8:g.122434719C=	NCBI36
NG_029473.1:g.8336G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1353G= MANE Select	ENSP00000432083.1:p.Lys451=
ENST00000227378.7:c.1353G=	ENSP00000227378.3:p.Lys451=
ENST00000453788.6:c.1353G=	ENSP00000404372.2:p.Lys451=
ENST00000524552.5:c.126G=	ENSP00000435908.1:p.Lys42=
ENST00000526110.5:c.1296G=	ENSP00000433584.1:p.Lys432=
ENST00000526686.1:c.9G=	ENSP00000435019.1:p.Lys3=
ENST00000532091.1:n.1328G=
ENST00000532636.5:c.1353G=	ENSP00000437125.1:p.Lys451=
ENST00000533238.5:n.455G=
ENST00000533540.5:c.915G=	ENSP00000437189.1:p.Lys305=
ENST00000534319.5:c.645G=	ENSP00000433316.1:p.Lys215=
ENST00000534624.5:c.1353G=	ENSP00000432083.1:p.Lys451=
NM_006597.5:c.1353G=	NP_006588.1:p.Lys451=
NM_153201.3:c.1353G=	NP_694881.1:p.Lys451=
XM_011542798.1:c.1353G=	XP_011541100.1:p.Lys451=
NM_006597.6:c.1353G= MANE Select	NP_006588.1:p.Lys451=
NM_153201.4:c.1353G=	NP_694881.1:p.Lys451=