Canonical Allele Identifier: CA2005595828

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058871G= , CM000673.2:g.123058871G=	GRCh38
NC_000011.9:g.122929579G= , CM000673.1:g.122929579G=	GRCh37
NC_000011.8:g.122434789G=	NCBI36
NG_029473.1:g.8266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-41C= MANE Select	ENSP00000432083.1:n.1324-41C=
ENST00000227378.7:c.1324-41C=	ENSP00000227378.3:n.1324-41C=
ENST00000453788.6:c.1324-41C=	ENSP00000404372.2:n.1324-41C=
ENST00000524552.5:c.97-41C=	ENSP00000435908.1:n.97-41C=
ENST00000526110.5:c.1267-41C=	ENSP00000433584.1:n.1267-41C=
ENST00000526686.1:c.-62C=	ENSP00000435019.1:n.-62C=
ENST00000532091.1:n.1258C=
ENST00000532636.5:c.1324-41C=	ENSP00000437125.1:n.1324-41C=
ENST00000533238.5:n.426-41C=
ENST00000533540.5:c.886-41C=	ENSP00000437189.1:n.886-41C=
ENST00000534319.5:c.616-41C=	ENSP00000433316.1:n.616-41C=
ENST00000534624.5:c.1324-41C=	ENSP00000432083.1:n.1324-41C=
NM_006597.5:c.1324-41C=	NP_006588.1:n.1324-41C=
NM_153201.3:c.1324-41C=	NP_694881.1:n.1324-41C=
XM_011542798.1:c.1324-41C=	XP_011541100.1:n.1324-41C=
NM_006597.6:c.1324-41C= MANE Select	NP_006588.1:n.1324-41C=
NM_153201.4:c.1324-41C=	NP_694881.1:n.1324-41C=