Canonical Allele Identifier: CA2005596461

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059024T= , CM000673.2:g.123059024T=	GRCh38
NC_000011.9:g.122929732T= , CM000673.1:g.122929732T=	GRCh37
NC_000011.8:g.122434942T=	NCBI36
NG_029473.1:g.8113A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+35A= MANE Select	ENSP00000432083.1:n.1323+35A=
ENST00000227378.7:c.1323+35A=	ENSP00000227378.3:n.1323+35A=
ENST00000453788.6:c.1323+35A=	ENSP00000404372.2:n.1323+35A=
ENST00000524552.5:c.96+35A=	ENSP00000435908.1:n.96+35A=
ENST00000526110.5:c.1266+35A=	ENSP00000433584.1:n.1266+35A=
ENST00000526686.1:c.-215A=	ENSP00000435019.1:n.-215A=
ENST00000532091.1:n.1105A=
ENST00000532636.5:c.1323+35A=	ENSP00000437125.1:n.1323+35A=
ENST00000533238.5:n.425+35A=
ENST00000533540.5:c.885+35A=	ENSP00000437189.1:n.885+35A=
ENST00000534319.5:c.615+35A=	ENSP00000433316.1:n.615+35A=
ENST00000534624.5:c.1323+35A=	ENSP00000432083.1:n.1323+35A=
NM_006597.5:c.1323+35A=	NP_006588.1:n.1323+35A=
NM_153201.3:c.1323+35A=	NP_694881.1:n.1323+35A=
XM_011542798.1:c.1323+35A=	XP_011541100.1:n.1323+35A=
NM_006597.6:c.1323+35A= MANE Select	NP_006588.1:n.1323+35A=
NM_153201.4:c.1323+35A=	NP_694881.1:n.1323+35A=