Canonical Allele Identifier: CA229967447

Gene: HSPA8

Linked Data

• dbSNP Id: rs899124471
• gnomAD v2: 11-122930029-GTT-G
• gnomAD v3: 11-123059321-GTT-G
• gnomAD v4: 11-123059321-GTT-G
• MyVariant Identifiers: chr11:g.122930030_122930031del (hg19) ; chr11:g.123059322_123059323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059324_123059325del , CM000673.2:g.123059324_123059325del	GRCh38
NC_000011.9:g.122930032_122930033del , CM000673.1:g.122930032_122930033del	GRCh37
NC_000011.8:g.122435242_122435243del	NCBI36
NG_029473.1:g.7814_7815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-62_1121-61del MANE Select	ENSP00000432083.1:n.1121-62_1121-61del
ENST00000227378.7:c.1121-62_1121-61del	ENSP00000227378.3:n.1121-62_1121-61del
ENST00000453788.6:c.1121-62_1121-61del	ENSP00000404372.2:n.1121-62_1121-61del
ENST00000524552.5:c.-169_-168del	ENSP00000435908.1:n.-169_-168del
ENST00000526110.5:c.1064-62_1064-61del	ENSP00000433584.1:n.1064-62_1064-61del
ENST00000526862.1:n.399-62_399-61del
ENST00000527983.5:n.1419_1420del
ENST00000532091.1:n.868-62_868-61del
ENST00000532636.5:c.1121-62_1121-61del	ENSP00000437125.1:n.1121-62_1121-61del
ENST00000533238.5:n.381-220_381-219del
ENST00000533540.5:c.683-62_683-61del	ENSP00000437189.1:n.683-62_683-61del
ENST00000534319.5:c.413-62_413-61del	ENSP00000433316.1:n.413-62_413-61del
ENST00000534624.5:c.1121-62_1121-61del	ENSP00000432083.1:n.1121-62_1121-61del
NM_006597.5:c.1121-62_1121-61del	NP_006588.1:n.1121-62_1121-61del
NM_153201.3:c.1121-62_1121-61del	NP_694881.1:n.1121-62_1121-61del
XM_011542798.1:c.1121-62_1121-61del	XP_011541100.1:n.1121-62_1121-61del
NM_006597.6:c.1121-62_1121-61del MANE Select	NP_006588.1:n.1121-62_1121-61del
NM_153201.4:c.1121-62_1121-61del	NP_694881.1:n.1121-62_1121-61del