Canonical Allele Identifier: CA477385763

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123059290-A-C
• MyVariant Identifiers: chr11:g.122929998A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059290A>C , CM000673.2:g.123059290A>C	GRCh38
NC_000011.9:g.122929998A>C , CM000673.1:g.122929998A>C	GRCh37
NC_000011.8:g.122435208A>C	NCBI36
NG_029473.1:g.7847T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-29T>G MANE Select	ENSP00000432083.1:n.1121-29T>G
ENST00000227378.7:c.1121-29T>G	ENSP00000227378.3:n.1121-29T>G
ENST00000453788.6:c.1121-29T>G	ENSP00000404372.2:n.1121-29T>G
ENST00000524552.5:c.-136T>G	ENSP00000435908.1:n.-136T>G
ENST00000526110.5:c.1064-29T>G	ENSP00000433584.1:n.1064-29T>G
ENST00000526862.1:n.399-29T>G
ENST00000527983.5:n.1452T>G
ENST00000532091.1:n.868-29T>G
ENST00000532636.5:c.1121-29T>G	ENSP00000437125.1:n.1121-29T>G
ENST00000533238.5:n.381-187T>G
ENST00000533540.5:c.683-29T>G	ENSP00000437189.1:n.683-29T>G
ENST00000534319.5:c.413-29T>G	ENSP00000433316.1:n.413-29T>G
ENST00000534624.5:c.1121-29T>G	ENSP00000432083.1:n.1121-29T>G
NM_006597.5:c.1121-29T>G	NP_006588.1:n.1121-29T>G
NM_153201.3:c.1121-29T>G	NP_694881.1:n.1121-29T>G
XM_011542798.1:c.1121-29T>G	XP_011541100.1:n.1121-29T>G
NM_006597.6:c.1121-29T>G MANE Select	NP_006588.1:n.1121-29T>G
NM_153201.4:c.1121-29T>G	NP_694881.1:n.1121-29T>G