Canonical Allele Identifier: CA2005595157

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058592C= , CM000673.2:g.123058592C=	GRCh38
NC_000011.9:g.122929300C= , CM000673.1:g.122929300C=	GRCh37
NC_000011.8:g.122434510C=	NCBI36
NG_029473.1:g.8545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+40G= MANE Select	ENSP00000432083.1:n.1522+40G=
ENST00000227378.7:c.1522+40G=	ENSP00000227378.3:n.1522+40G=
ENST00000453788.6:c.1387+175G=	ENSP00000404372.2:n.1387+175G=
ENST00000524552.5:c.295+40G=	ENSP00000435908.1:n.295+40G=
ENST00000526110.5:c.1465+40G=	ENSP00000433584.1:n.1465+40G=
ENST00000526686.1:c.178+40G=	ENSP00000435019.1:n.178+40G=
ENST00000532091.1:n.1537G=
ENST00000532636.5:c.1522+40G=	ENSP00000437125.1:n.1522+40G=
ENST00000533540.5:c.1084+40G=	ENSP00000437189.1:n.1084+40G=
ENST00000534319.5:c.814+40G=	ENSP00000433316.1:n.814+40G=
ENST00000534624.5:c.1522+40G=	ENSP00000432083.1:n.1522+40G=
NM_006597.5:c.1522+40G=	NP_006588.1:n.1522+40G=
NM_153201.3:c.1387+175G=	NP_694881.1:n.1387+175G=
XM_011542798.1:c.1522+40G=	XP_011541100.1:n.1522+40G=
NM_006597.6:c.1522+40G= MANE Select	NP_006588.1:n.1522+40G=
NM_153201.4:c.1387+175G=	NP_694881.1:n.1387+175G=