Canonical Allele Identifier: CA477385718

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929944T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059236T>G , CM000673.2:g.123059236T>G	GRCh38
NC_000011.9:g.122929944T>G , CM000673.1:g.122929944T>G	GRCh37
NC_000011.8:g.122435154T>G	NCBI36
NG_029473.1:g.7901A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1146A>C MANE Select	ENSP00000432083.1:p.Gly382=
ENST00000227378.7:c.1146A>C	ENSP00000227378.3:p.Gly382=
ENST00000453788.6:c.1146A>C	ENSP00000404372.2:p.Gly382=
ENST00000524552.5:c.-82A>C	ENSP00000435908.1:n.-82A>C
ENST00000526110.5:c.1089A>C	ENSP00000433584.1:p.Gly363=
ENST00000526862.1:n.424A>C
ENST00000527983.5:n.1506A>C
ENST00000532091.1:n.893A>C
ENST00000532636.5:c.1146A>C	ENSP00000437125.1:p.Gly382=
ENST00000533238.5:n.381-133A>C
ENST00000533540.5:c.708A>C	ENSP00000437189.1:p.Gly236=
ENST00000534319.5:c.438A>C	ENSP00000433316.1:p.Gly146=
ENST00000534624.5:c.1146A>C	ENSP00000432083.1:p.Gly382=
NM_006597.5:c.1146A>C	NP_006588.1:p.Gly382=
NM_153201.3:c.1146A>C	NP_694881.1:p.Gly382=
XM_011542798.1:c.1146A>C	XP_011541100.1:p.Gly382=
NM_006597.6:c.1146A>C MANE Select	NP_006588.1:p.Gly382=
NM_153201.4:c.1146A>C	NP_694881.1:p.Gly382=