Canonical Allele Identifier: CA6332545

Gene: HSPA8

Linked Data

• dbSNP Id: rs764797484
• ExAC: 11:122929984 G / C
• gnomAD v2: 11-122929984-G-C
• gnomAD v4: 11-123059276-G-C
• MyVariant Identifiers: chr11:g.122929984G>C (hg19) ; chr11:g.123059276G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059276G>C , CM000673.2:g.123059276G>C	GRCh38
NC_000011.9:g.122929984G>C , CM000673.1:g.122929984G>C	GRCh37
NC_000011.8:g.122435194G>C	NCBI36
NG_029473.1:g.7861C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-15C>G MANE Select	ENSP00000432083.1:n.1121-15C>G
ENST00000227378.7:c.1121-15C>G	ENSP00000227378.3:n.1121-15C>G
ENST00000453788.6:c.1121-15C>G	ENSP00000404372.2:n.1121-15C>G
ENST00000524552.5:c.-122C>G	ENSP00000435908.1:n.-122C>G
ENST00000526110.5:c.1064-15C>G	ENSP00000433584.1:n.1064-15C>G
ENST00000526862.1:n.399-15C>G
ENST00000527983.5:n.1466C>G
ENST00000532091.1:n.868-15C>G
ENST00000532636.5:c.1121-15C>G	ENSP00000437125.1:n.1121-15C>G
ENST00000533238.5:n.381-173C>G
ENST00000533540.5:c.683-15C>G	ENSP00000437189.1:n.683-15C>G
ENST00000534319.5:c.413-15C>G	ENSP00000433316.1:n.413-15C>G
ENST00000534624.5:c.1121-15C>G	ENSP00000432083.1:n.1121-15C>G
NM_006597.5:c.1121-15C>G	NP_006588.1:n.1121-15C>G
NM_153201.3:c.1121-15C>G	NP_694881.1:n.1121-15C>G
XM_011542798.1:c.1121-15C>G	XP_011541100.1:n.1121-15C>G
NM_006597.6:c.1121-15C>G MANE Select	NP_006588.1:n.1121-15C>G
NM_153201.4:c.1121-15C>G	NP_694881.1:n.1121-15C>G