Canonical Allele Identifier: CA654591118

Gene: HSPA8

Linked Data

• COSMIC: COSN20055896

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058508_123058513del , CM000673.2:g.123058508_123058513del	GRCh38
NC_000011.9:g.122929216_122929221del , CM000673.1:g.122929216_122929221del	GRCh37
NC_000011.8:g.122434426_122434431del	NCBI36
NG_029473.1:g.8627_8632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-26_1523-21del MANE Select	ENSP00000432083.1:n.1523-26_1523-21del
ENST00000227378.7:c.1523-26_1523-21del	ENSP00000227378.3:n.1523-26_1523-21del
ENST00000453788.6:c.1387+257_1387+262del	ENSP00000404372.2:n.1387+257_1387+262del
ENST00000524552.5:c.296-26_296-21del	ENSP00000435908.1:n.296-26_296-21del
ENST00000526110.5:c.1466-26_1466-21del	ENSP00000433584.1:n.1466-26_1466-21del
ENST00000526686.1:c.179-26_179-21del	ENSP00000435019.1:n.179-26_179-21del
ENST00000532091.1:n.1619_1624del
ENST00000532636.5:c.1523-26_1523-21del	ENSP00000437125.1:n.1523-26_1523-21del
ENST00000533540.5:c.1085-26_1085-21del	ENSP00000437189.1:n.1085-26_1085-21del
ENST00000534319.5:c.815-26_815-21del	ENSP00000433316.1:n.815-26_815-21del
ENST00000534624.5:c.1523-26_1523-21del	ENSP00000432083.1:n.1523-26_1523-21del
NM_006597.5:c.1523-26_1523-21del	NP_006588.1:n.1523-26_1523-21del
NM_153201.3:c.1387+257_1387+262del	NP_694881.1:n.1387+257_1387+262del
XM_011542798.1:c.1523-26_1523-21del	XP_011541100.1:n.1523-26_1523-21del
NM_006597.6:c.1523-26_1523-21del MANE Select	NP_006588.1:n.1523-26_1523-21del
NM_153201.4:c.1387+257_1387+262del	NP_694881.1:n.1387+257_1387+262del