Canonical Allele Identifier: CA2616532779

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058610-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058611_123058612del , CM000673.2:g.123058611_123058612del	GRCh38
NC_000011.9:g.122929319_122929320del , CM000673.1:g.122929319_122929320del	GRCh37
NC_000011.8:g.122434529_122434530del	NCBI36
NG_029473.1:g.8525_8526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+20_1522+21del MANE Select	ENSP00000432083.1:n.1522+20_1522+21del
ENST00000227378.7:c.1522+20_1522+21del	ENSP00000227378.3:n.1522+20_1522+21del
ENST00000453788.6:c.1387+155_1387+156del	ENSP00000404372.2:n.1387+155_1387+156del
ENST00000524552.5:c.295+20_295+21del	ENSP00000435908.1:n.295+20_295+21del
ENST00000526110.5:c.1465+20_1465+21del	ENSP00000433584.1:n.1465+20_1465+21del
ENST00000526686.1:c.178+20_178+21del	ENSP00000435019.1:n.178+20_178+21del
ENST00000532091.1:n.1517_1518del
ENST00000532636.5:c.1522+20_1522+21del	ENSP00000437125.1:n.1522+20_1522+21del
ENST00000533540.5:c.1084+20_1084+21del	ENSP00000437189.1:n.1084+20_1084+21del
ENST00000534319.5:c.814+20_814+21del	ENSP00000433316.1:n.814+20_814+21del
ENST00000534624.5:c.1522+20_1522+21del	ENSP00000432083.1:n.1522+20_1522+21del
NM_006597.5:c.1522+20_1522+21del	NP_006588.1:n.1522+20_1522+21del
NM_153201.3:c.1387+155_1387+156del	NP_694881.1:n.1387+155_1387+156del
XM_011542798.1:c.1522+20_1522+21del	XP_011541100.1:n.1522+20_1522+21del
NM_006597.6:c.1522+20_1522+21del MANE Select	NP_006588.1:n.1522+20_1522+21del
NM_153201.4:c.1387+155_1387+156del	NP_694881.1:n.1387+155_1387+156del