Canonical Allele Identifier: CA602581114

Gene: HSPA8

Linked Data

• dbSNP Id: rs1294616349
• gnomAD v2: 11-122929994-AAAG-A
• gnomAD v3: 11-123059286-AAAG-A
• gnomAD v4: 11-123059286-AAAG-A
• MyVariant Identifiers: chr11:g.122929995_122929997del (hg19) ; chr11:g.123059287_123059289del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059290_123059292del , CM000673.2:g.123059290_123059292del	GRCh38
NC_000011.9:g.122929998_122930000del , CM000673.1:g.122929998_122930000del	GRCh37
NC_000011.8:g.122435208_122435210del	NCBI36
NG_029473.1:g.7848_7850del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-28_1121-26del MANE Select	ENSP00000432083.1:n.1121-28_1121-26del
ENST00000227378.7:c.1121-28_1121-26del	ENSP00000227378.3:n.1121-28_1121-26del
ENST00000453788.6:c.1121-28_1121-26del	ENSP00000404372.2:n.1121-28_1121-26del
ENST00000524552.5:c.-135_-133del	ENSP00000435908.1:n.-135_-133del
ENST00000526110.5:c.1064-28_1064-26del	ENSP00000433584.1:n.1064-28_1064-26del
ENST00000526862.1:n.399-28_399-26del
ENST00000527983.5:n.1453_1455del
ENST00000532091.1:n.868-28_868-26del
ENST00000532636.5:c.1121-28_1121-26del	ENSP00000437125.1:n.1121-28_1121-26del
ENST00000533238.5:n.381-186_381-184del
ENST00000533540.5:c.683-28_683-26del	ENSP00000437189.1:n.683-28_683-26del
ENST00000534319.5:c.413-28_413-26del	ENSP00000433316.1:n.413-28_413-26del
ENST00000534624.5:c.1121-28_1121-26del	ENSP00000432083.1:n.1121-28_1121-26del
NM_006597.5:c.1121-28_1121-26del	NP_006588.1:n.1121-28_1121-26del
NM_153201.3:c.1121-28_1121-26del	NP_694881.1:n.1121-28_1121-26del
XM_011542798.1:c.1121-28_1121-26del	XP_011541100.1:n.1121-28_1121-26del
NM_006597.6:c.1121-28_1121-26del MANE Select	NP_006588.1:n.1121-28_1121-26del
NM_153201.4:c.1121-28_1121-26del	NP_694881.1:n.1121-28_1121-26del