Canonical Allele Identifier: CA383057261

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929433T>G (hg19) ; chr11:g.123058725T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058725T>G , CM000673.2:g.123058725T>G	GRCh38
NC_000011.9:g.122929433T>G , CM000673.1:g.122929433T>G	GRCh37
NC_000011.8:g.122434643T>G	NCBI36
NG_029473.1:g.8412A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1429A>C MANE Select	ENSP00000432083.1:p.Thr477Pro
ENST00000227378.7:c.1429A>C	ENSP00000227378.3:p.Thr477Pro
ENST00000453788.6:c.1387+42A>C	ENSP00000404372.2:n.1387+42A>C
ENST00000524552.5:c.202A>C	ENSP00000435908.1:p.Thr68Pro
ENST00000526110.5:c.1372A>C	ENSP00000433584.1:p.Thr458Pro
ENST00000526686.1:c.85A>C	ENSP00000435019.1:p.Thr29Pro
ENST00000532091.1:n.1404A>C
ENST00000532636.5:c.1429A>C	ENSP00000437125.1:p.Thr477Pro
ENST00000533540.5:c.991A>C	ENSP00000437189.1:p.Thr331Pro
ENST00000534319.5:c.721A>C	ENSP00000433316.1:p.Thr241Pro
ENST00000534624.5:c.1429A>C	ENSP00000432083.1:p.Thr477Pro
NM_006597.5:c.1429A>C	NP_006588.1:p.Thr477Pro
NM_153201.3:c.1387+42A>C	NP_694881.1:n.1387+42A>C
XM_011542798.1:c.1429A>C	XP_011541100.1:p.Thr477Pro
NM_006597.6:c.1429A>C MANE Select	NP_006588.1:p.Thr477Pro
NM_153201.4:c.1387+42A>C	NP_694881.1:n.1387+42A>C