Canonical Allele Identifier: CA672749163

Gene: HSPA8

Linked Data

• dbSNP Id: rs1420575637
• gnomAD v4: 11-123059037-CAAGAG-C
• MyVariant Identifiers: chr11:g.122929746_122929750del (hg19) ; chr11:g.123059038_123059042del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059041_123059045del , CM000673.2:g.123059041_123059045del	GRCh38
NC_000011.9:g.122929749_122929753del , CM000673.1:g.122929749_122929753del	GRCh37
NC_000011.8:g.122434959_122434963del	NCBI36
NG_029473.1:g.8095_8099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+17_1323+21del MANE Select	ENSP00000432083.1:n.1323+17_1323+21del
ENST00000227378.7:c.1323+17_1323+21del	ENSP00000227378.3:n.1323+17_1323+21del
ENST00000453788.6:c.1323+17_1323+21del	ENSP00000404372.2:n.1323+17_1323+21del
ENST00000524552.5:c.96+17_96+21del	ENSP00000435908.1:n.96+17_96+21del
ENST00000526110.5:c.1266+17_1266+21del	ENSP00000433584.1:n.1266+17_1266+21del
ENST00000526686.1:c.-233_-229del	ENSP00000435019.1:n.-233_-229del
ENST00000532091.1:n.1087_1091del
ENST00000532636.5:c.1323+17_1323+21del	ENSP00000437125.1:n.1323+17_1323+21del
ENST00000533238.5:n.425+17_425+21del
ENST00000533540.5:c.885+17_885+21del	ENSP00000437189.1:n.885+17_885+21del
ENST00000534319.5:c.615+17_615+21del	ENSP00000433316.1:n.615+17_615+21del
ENST00000534624.5:c.1323+17_1323+21del	ENSP00000432083.1:n.1323+17_1323+21del
NM_006597.5:c.1323+17_1323+21del	NP_006588.1:n.1323+17_1323+21del
NM_153201.3:c.1323+17_1323+21del	NP_694881.1:n.1323+17_1323+21del
XM_011542798.1:c.1323+17_1323+21del	XP_011541100.1:n.1323+17_1323+21del
NM_006597.6:c.1323+17_1323+21del MANE Select	NP_006588.1:n.1323+17_1323+21del
NM_153201.4:c.1323+17_1323+21del	NP_694881.1:n.1323+17_1323+21del