Canonical Allele Identifier: CA602581185

Gene: HSPA8

Linked Data

• dbSNP Id: rs1565367239
• gnomAD v2: 11-122929577-AG-A
• gnomAD v4: 11-123058869-AG-A
• MyVariant Identifiers: chr11:g.122929578del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058871del , CM000673.2:g.123058871del	GRCh38
NC_000011.9:g.122929579del , CM000673.1:g.122929579del	GRCh37
NC_000011.8:g.122434789del	NCBI36
NG_029473.1:g.8267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-40del MANE Select	ENSP00000432083.1:n.1324-40del
ENST00000227378.7:c.1324-40del	ENSP00000227378.3:n.1324-40del
ENST00000453788.6:c.1324-40del	ENSP00000404372.2:n.1324-40del
ENST00000524552.5:c.97-40del	ENSP00000435908.1:n.97-40del
ENST00000526110.5:c.1267-40del	ENSP00000433584.1:n.1267-40del
ENST00000526686.1:c.-61del	ENSP00000435019.1:n.-61del
ENST00000532091.1:n.1259del
ENST00000532636.5:c.1324-40del	ENSP00000437125.1:n.1324-40del
ENST00000533238.5:n.426-40del
ENST00000533540.5:c.886-40del	ENSP00000437189.1:n.886-40del
ENST00000534319.5:c.616-40del	ENSP00000433316.1:n.616-40del
ENST00000534624.5:c.1324-40del	ENSP00000432083.1:n.1324-40del
NM_006597.5:c.1324-40del	NP_006588.1:n.1324-40del
NM_153201.3:c.1324-40del	NP_694881.1:n.1324-40del
XM_011542798.1:c.1324-40del	XP_011541100.1:n.1324-40del
NM_006597.6:c.1324-40del MANE Select	NP_006588.1:n.1324-40del
NM_153201.4:c.1324-40del	NP_694881.1:n.1324-40del