Canonical Allele Identifier: CA2005597160

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059245G= , CM000673.2:g.123059245G=	GRCh38
NC_000011.9:g.122929953G= , CM000673.1:g.122929953G=	GRCh37
NC_000011.8:g.122435163G=	NCBI36
NG_029473.1:g.7892C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1137C= MANE Select	ENSP00000432083.1:p.Ile379=
ENST00000227378.7:c.1137C=	ENSP00000227378.3:p.Ile379=
ENST00000453788.6:c.1137C=	ENSP00000404372.2:p.Ile379=
ENST00000524552.5:c.-91C=	ENSP00000435908.1:n.-91C=
ENST00000526110.5:c.1080C=	ENSP00000433584.1:p.Ile360=
ENST00000526862.1:n.415C=
ENST00000527983.5:n.1497C=
ENST00000532091.1:n.884C=
ENST00000532636.5:c.1137C=	ENSP00000437125.1:p.Ile379=
ENST00000533238.5:n.381-142C=
ENST00000533540.5:c.699C=	ENSP00000437189.1:p.Ile233=
ENST00000534319.5:c.429C=	ENSP00000433316.1:p.Ile143=
ENST00000534624.5:c.1137C=	ENSP00000432083.1:p.Ile379=
NM_006597.5:c.1137C=	NP_006588.1:p.Ile379=
NM_153201.3:c.1137C=	NP_694881.1:p.Ile379=
XM_011542798.1:c.1137C=	XP_011541100.1:p.Ile379=
NM_006597.6:c.1137C= MANE Select	NP_006588.1:p.Ile379=
NM_153201.4:c.1137C=	NP_694881.1:p.Ile379=