Canonical Allele Identifier: CA6332496

Gene: HSPA8

Linked Data

• dbSNP Id: rs754334609
• ExAC: 11:122929576 CAGGTCTGTGACAGTGCTAGGGTCCTGCTAAGGAAGA / C
• gnomAD v2: 11-122929576-CAGGTCTGTGACAGTGCTAGGGTCCTGCTAAGGAAGA-C
• gnomAD v3: 11-123058868-CAGGTCTGTGACAGTGCTAGGGTCCTGCTAAGGAAGA-C
• gnomAD v4: 11-123058868-CAGGTCTGTGACAGTGCTAGGGTCCTGCTAAGGAAGA-C
• MyVariant Identifiers: chr11:g.122929577_122929612del (hg19) ; chr11:g.123058869_123058904del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058870_123058905del , CM000673.2:g.123058870_123058905del	GRCh38
NC_000011.9:g.122929578_122929613del , CM000673.1:g.122929578_122929613del	GRCh37
NC_000011.8:g.122434788_122434823del	NCBI36
NG_029473.1:g.8233_8268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-74_1324-39del MANE Select	ENSP00000432083.1:n.1324-74_1324-39del
ENST00000227378.7:c.1324-74_1324-39del	ENSP00000227378.3:n.1324-74_1324-39del
ENST00000453788.6:c.1324-74_1324-39del	ENSP00000404372.2:n.1324-74_1324-39del
ENST00000524552.5:c.97-74_97-39del	ENSP00000435908.1:n.97-74_97-39del
ENST00000526110.5:c.1267-74_1267-39del	ENSP00000433584.1:n.1267-74_1267-39del
ENST00000526686.1:c.-95_-60del	ENSP00000435019.1:n.-95_-60del
ENST00000532091.1:n.1225_1260del
ENST00000532636.5:c.1324-74_1324-39del	ENSP00000437125.1:n.1324-74_1324-39del
ENST00000533238.5:n.426-74_426-39del
ENST00000533540.5:c.886-74_886-39del	ENSP00000437189.1:n.886-74_886-39del
ENST00000534319.5:c.616-74_616-39del	ENSP00000433316.1:n.616-74_616-39del
ENST00000534624.5:c.1324-74_1324-39del	ENSP00000432083.1:n.1324-74_1324-39del
NM_006597.5:c.1324-74_1324-39del	NP_006588.1:n.1324-74_1324-39del
NM_153201.3:c.1324-74_1324-39del	NP_694881.1:n.1324-74_1324-39del
XM_011542798.1:c.1324-74_1324-39del	XP_011541100.1:n.1324-74_1324-39del
NM_006597.6:c.1324-74_1324-39del MANE Select	NP_006588.1:n.1324-74_1324-39del
NM_153201.4:c.1324-74_1324-39del	NP_694881.1:n.1324-74_1324-39del