Canonical Allele Identifier: CA943028073

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865419515
• gnomAD v3: 11-123059308-G-GTACA
• gnomAD v4: 11-123059308-G-GTACA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059311_123059314dup , CM000673.2:g.123059311_123059314dup	GRCh38
NC_000011.9:g.122930019_122930022dup , CM000673.1:g.122930019_122930022dup	GRCh37
NC_000011.8:g.122435229_122435232dup	NCBI36
NG_029473.1:g.7825_7828dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-51_1121-48dup MANE Select	ENSP00000432083.1:n.1121-51_1121-48dup
ENST00000227378.7:c.1121-51_1121-48dup	ENSP00000227378.3:n.1121-51_1121-48dup
ENST00000453788.6:c.1121-51_1121-48dup	ENSP00000404372.2:n.1121-51_1121-48dup
ENST00000524552.5:c.-158_-155dup	ENSP00000435908.1:n.-158_-155dup
ENST00000526110.5:c.1064-51_1064-48dup	ENSP00000433584.1:n.1064-51_1064-48dup
ENST00000526862.1:n.399-51_399-48dup
ENST00000527983.5:n.1430_1433dup
ENST00000532091.1:n.868-51_868-48dup
ENST00000532636.5:c.1121-51_1121-48dup	ENSP00000437125.1:n.1121-51_1121-48dup
ENST00000533238.5:n.381-209_381-206dup
ENST00000533540.5:c.683-51_683-48dup	ENSP00000437189.1:n.683-51_683-48dup
ENST00000534319.5:c.413-51_413-48dup	ENSP00000433316.1:n.413-51_413-48dup
ENST00000534624.5:c.1121-51_1121-48dup	ENSP00000432083.1:n.1121-51_1121-48dup
NM_006597.5:c.1121-51_1121-48dup	NP_006588.1:n.1121-51_1121-48dup
NM_153201.3:c.1121-51_1121-48dup	NP_694881.1:n.1121-51_1121-48dup
XM_011542798.1:c.1121-51_1121-48dup	XP_011541100.1:n.1121-51_1121-48dup
NM_006597.6:c.1121-51_1121-48dup MANE Select	NP_006588.1:n.1121-51_1121-48dup
NM_153201.4:c.1121-51_1121-48dup	NP_694881.1:n.1121-51_1121-48dup