Canonical Allele Identifier: CA943027838

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865398780
• gnomAD v3: 11-123058891-CCTG-C
• gnomAD v4: 11-123058891-CCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058894_123058896del , CM000673.2:g.123058894_123058896del	GRCh38
NC_000011.9:g.122929602_122929604del , CM000673.1:g.122929602_122929604del	GRCh37
NC_000011.8:g.122434812_122434814del	NCBI36
NG_029473.1:g.8243_8245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-64_1324-62del MANE Select	ENSP00000432083.1:n.1324-64_1324-62del
ENST00000227378.7:c.1324-64_1324-62del	ENSP00000227378.3:n.1324-64_1324-62del
ENST00000453788.6:c.1324-64_1324-62del	ENSP00000404372.2:n.1324-64_1324-62del
ENST00000524552.5:c.97-64_97-62del	ENSP00000435908.1:n.97-64_97-62del
ENST00000526110.5:c.1267-64_1267-62del	ENSP00000433584.1:n.1267-64_1267-62del
ENST00000526686.1:c.-85_-83del	ENSP00000435019.1:n.-85_-83del
ENST00000532091.1:n.1235_1237del
ENST00000532636.5:c.1324-64_1324-62del	ENSP00000437125.1:n.1324-64_1324-62del
ENST00000533238.5:n.426-64_426-62del
ENST00000533540.5:c.886-64_886-62del	ENSP00000437189.1:n.886-64_886-62del
ENST00000534319.5:c.616-64_616-62del	ENSP00000433316.1:n.616-64_616-62del
ENST00000534624.5:c.1324-64_1324-62del	ENSP00000432083.1:n.1324-64_1324-62del
NM_006597.5:c.1324-64_1324-62del	NP_006588.1:n.1324-64_1324-62del
NM_153201.3:c.1324-64_1324-62del	NP_694881.1:n.1324-64_1324-62del
XM_011542798.1:c.1324-64_1324-62del	XP_011541100.1:n.1324-64_1324-62del
NM_006597.6:c.1324-64_1324-62del MANE Select	NP_006588.1:n.1324-64_1324-62del
NM_153201.4:c.1324-64_1324-62del	NP_694881.1:n.1324-64_1324-62del