Canonical Allele Identifier: CA2005595448

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058720A= , CM000673.2:g.123058720A=	GRCh38
NC_000011.9:g.122929428A= , CM000673.1:g.122929428A=	GRCh37
NC_000011.8:g.122434638A=	NCBI36
NG_029473.1:g.8417T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1434T= MANE Select	ENSP00000432083.1:p.Phe478=
ENST00000227378.7:c.1434T=	ENSP00000227378.3:p.Phe478=
ENST00000453788.6:c.1387+47T=	ENSP00000404372.2:n.1387+47T=
ENST00000524552.5:c.207T=	ENSP00000435908.1:p.Phe69=
ENST00000526110.5:c.1377T=	ENSP00000433584.1:p.Phe459=
ENST00000526686.1:c.90T=	ENSP00000435019.1:p.Phe30=
ENST00000532091.1:n.1409T=
ENST00000532636.5:c.1434T=	ENSP00000437125.1:p.Phe478=
ENST00000533540.5:c.996T=	ENSP00000437189.1:p.Phe332=
ENST00000534319.5:c.726T=	ENSP00000433316.1:p.Phe242=
ENST00000534624.5:c.1434T=	ENSP00000432083.1:p.Phe478=
NM_006597.5:c.1434T=	NP_006588.1:p.Phe478=
NM_153201.3:c.1387+47T=	NP_694881.1:n.1387+47T=
XM_011542798.1:c.1434T=	XP_011541100.1:p.Phe478=
NM_006597.6:c.1434T= MANE Select	NP_006588.1:p.Phe478=
NM_153201.4:c.1387+47T=	NP_694881.1:n.1387+47T=