Canonical Allele Identifier: CA6332462

Gene: HSPA8

Linked Data

• dbSNP Id: rs766069802
• ExAC: 11:122929351 G / C
• gnomAD v2: 11-122929351-G-C
• gnomAD v4: 11-123058643-G-C
• MyVariant Identifiers: chr11:g.122929351G>C (hg19) ; chr11:g.123058643G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058643G>C , CM000673.2:g.123058643G>C	GRCh38
NC_000011.9:g.122929351G>C , CM000673.1:g.122929351G>C	GRCh37
NC_000011.8:g.122434561G>C	NCBI36
NG_029473.1:g.8494C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1511C>G MANE Select	ENSP00000432083.1:p.Thr504Ser
ENST00000227378.7:c.1511C>G	ENSP00000227378.3:p.Thr504Ser
ENST00000453788.6:c.1387+124C>G	ENSP00000404372.2:n.1387+124C>G
ENST00000524552.5:c.284C>G	ENSP00000435908.1:p.Thr95Ser
ENST00000526110.5:c.1454C>G	ENSP00000433584.1:p.Thr485Ser
ENST00000526686.1:c.167C>G	ENSP00000435019.1:p.Thr56Ser
ENST00000532091.1:n.1486C>G
ENST00000532636.5:c.1511C>G	ENSP00000437125.1:p.Thr504Ser
ENST00000533540.5:c.1073C>G	ENSP00000437189.1:p.Thr358Ser
ENST00000534319.5:c.803C>G	ENSP00000433316.1:p.Thr268Ser
ENST00000534624.5:c.1511C>G	ENSP00000432083.1:p.Thr504Ser
NM_006597.5:c.1511C>G	NP_006588.1:p.Thr504Ser
NM_153201.3:c.1387+124C>G	NP_694881.1:n.1387+124C>G
XM_011542798.1:c.1511C>G	XP_011541100.1:p.Thr504Ser
NM_006597.6:c.1511C>G MANE Select	NP_006588.1:p.Thr504Ser
NM_153201.4:c.1387+124C>G	NP_694881.1:n.1387+124C>G