Canonical Allele Identifier: CA2616532859

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123059005-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059006_123059007del , CM000673.2:g.123059006_123059007del	GRCh38
NC_000011.9:g.122929714_122929715del , CM000673.1:g.122929714_122929715del	GRCh37
NC_000011.8:g.122434924_122434925del	NCBI36
NG_029473.1:g.8130_8131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+52_1323+53del MANE Select	ENSP00000432083.1:n.1323+52_1323+53del
ENST00000227378.7:c.1323+52_1323+53del	ENSP00000227378.3:n.1323+52_1323+53del
ENST00000453788.6:c.1323+52_1323+53del	ENSP00000404372.2:n.1323+52_1323+53del
ENST00000524552.5:c.96+52_96+53del	ENSP00000435908.1:n.96+52_96+53del
ENST00000526110.5:c.1266+52_1266+53del	ENSP00000433584.1:n.1266+52_1266+53del
ENST00000526686.1:c.-198_-197del	ENSP00000435019.1:n.-198_-197del
ENST00000532091.1:n.1122_1123del
ENST00000532636.5:c.1323+52_1323+53del	ENSP00000437125.1:n.1323+52_1323+53del
ENST00000533238.5:n.425+52_425+53del
ENST00000533540.5:c.885+52_885+53del	ENSP00000437189.1:n.885+52_885+53del
ENST00000534319.5:c.615+52_615+53del	ENSP00000433316.1:n.615+52_615+53del
ENST00000534624.5:c.1323+52_1323+53del	ENSP00000432083.1:n.1323+52_1323+53del
NM_006597.5:c.1323+52_1323+53del	NP_006588.1:n.1323+52_1323+53del
NM_153201.3:c.1323+52_1323+53del	NP_694881.1:n.1323+52_1323+53del
XM_011542798.1:c.1323+52_1323+53del	XP_011541100.1:n.1323+52_1323+53del
NM_006597.6:c.1323+52_1323+53del MANE Select	NP_006588.1:n.1323+52_1323+53del
NM_153201.4:c.1323+52_1323+53del	NP_694881.1:n.1323+52_1323+53del