Canonical Allele Identifier: CA2005597153

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865415525

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059241del , CM000673.2:g.123059241del	GRCh38
NC_000011.9:g.122929949del , CM000673.1:g.122929949del	GRCh37
NC_000011.8:g.122435159del	NCBI36
NG_029473.1:g.7896del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1141del MANE Select	ENSP00000432083.1:p.Ser381LeufsTer30
ENST00000227378.7:c.1141del	ENSP00000227378.3:p.Ser381LeufsTer30
ENST00000453788.6:c.1141del	ENSP00000404372.2:p.Ser381LeufsTer30
ENST00000524552.5:c.-87del	ENSP00000435908.1:n.-87del
ENST00000526110.5:c.1084del	ENSP00000433584.1:p.Ser362LeufsTer30
ENST00000526862.1:n.419del
ENST00000527983.5:n.1501del
ENST00000532091.1:n.888del
ENST00000532636.5:c.1141del	ENSP00000437125.1:p.Ser381LeufsTer30
ENST00000533238.5:n.381-138del
ENST00000533540.5:c.703del	ENSP00000437189.1:p.Ser235LeufsTer30
ENST00000534319.5:c.433del	ENSP00000433316.1:p.Ser145LeufsTer30
ENST00000534624.5:c.1141del	ENSP00000432083.1:p.Ser381LeufsTer30
NM_006597.5:c.1141del	NP_006588.1:p.Ser381LeufsTer30
NM_153201.3:c.1141del	NP_694881.1:p.Ser381LeufsTer30
XM_011542798.1:c.1141del	XP_011541100.1:p.Ser381LeufsTer30
NM_006597.6:c.1141del MANE Select	NP_006588.1:p.Ser381LeufsTer30
NM_153201.4:c.1141del	NP_694881.1:p.Ser381LeufsTer30