Canonical Allele Identifier: CA2005596967

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059175T= , CM000673.2:g.123059175T=	GRCh38
NC_000011.9:g.122929883T= , CM000673.1:g.122929883T=	GRCh37
NC_000011.8:g.122435093T=	NCBI36
NG_029473.1:g.7962A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1207A= MANE Select	ENSP00000432083.1:p.Ile403=
ENST00000227378.7:c.1207A=	ENSP00000227378.3:p.Ile403=
ENST00000453788.6:c.1207A=	ENSP00000404372.2:p.Ile403=
ENST00000524552.5:c.-21A=	ENSP00000435908.1:n.-21A=
ENST00000526110.5:c.1150A=	ENSP00000433584.1:p.Ile384=
ENST00000526862.1:n.485A=
ENST00000532091.1:n.954A=
ENST00000532636.5:c.1207A=	ENSP00000437125.1:p.Ile403=
ENST00000533238.5:n.381-72A=
ENST00000533540.5:c.769A=	ENSP00000437189.1:p.Ile257=
ENST00000534319.5:c.499A=	ENSP00000433316.1:p.Ile167=
ENST00000534624.5:c.1207A=	ENSP00000432083.1:p.Ile403=
NM_006597.5:c.1207A=	NP_006588.1:p.Ile403=
NM_153201.3:c.1207A=	NP_694881.1:p.Ile403=
XM_011542798.1:c.1207A=	XP_011541100.1:p.Ile403=
NM_006597.6:c.1207A= MANE Select	NP_006588.1:p.Ile403=
NM_153201.4:c.1207A=	NP_694881.1:p.Ile403=