Canonical Allele Identifier: CA2616532795

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058719-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058722_123058723del , CM000673.2:g.123058722_123058723del	GRCh38
NC_000011.9:g.122929430_122929431del , CM000673.1:g.122929430_122929431del	GRCh37
NC_000011.8:g.122434640_122434641del	NCBI36
NG_029473.1:g.8416_8417del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1433_1434del MANE Select	ENSP00000432083.1:p.Phe478Ter
ENST00000227378.7:c.1433_1434del	ENSP00000227378.3:p.Phe478Ter
ENST00000453788.6:c.1387+46_1387+47del	ENSP00000404372.2:n.1387+46_1387+47del
ENST00000524552.5:c.206_207del	ENSP00000435908.1:p.Phe69Ter
ENST00000526110.5:c.1376_1377del	ENSP00000433584.1:p.Phe459Ter
ENST00000526686.1:c.89_90del	ENSP00000435019.1:p.Phe30Ter
ENST00000532091.1:n.1408_1409del
ENST00000532636.5:c.1433_1434del	ENSP00000437125.1:p.Phe478Ter
ENST00000533540.5:c.995_996del	ENSP00000437189.1:p.Phe332Ter
ENST00000534319.5:c.725_726del	ENSP00000433316.1:p.Phe242Ter
ENST00000534624.5:c.1433_1434del	ENSP00000432083.1:p.Phe478Ter
NM_006597.5:c.1433_1434del	NP_006588.1:p.Phe478Ter
NM_153201.3:c.1387+46_1387+47del	NP_694881.1:n.1387+46_1387+47del
XM_011542798.1:c.1433_1434del	XP_011541100.1:p.Phe478Ter
NM_006597.6:c.1433_1434del MANE Select	NP_006588.1:p.Phe478Ter
NM_153201.4:c.1387+46_1387+47del	NP_694881.1:n.1387+46_1387+47del