Canonical Allele Identifier: CA2005595269

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865392085

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058626_123058628del , CM000673.2:g.123058626_123058628del	GRCh38
NC_000011.9:g.122929334_122929336del , CM000673.1:g.122929334_122929336del	GRCh37
NC_000011.8:g.122434544_122434546del	NCBI36
NG_029473.1:g.8512_8514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+7_1522+9del MANE Select	ENSP00000432083.1:n.1522+7_1522+9del
ENST00000227378.7:c.1522+7_1522+9del	ENSP00000227378.3:n.1522+7_1522+9del
ENST00000453788.6:c.1387+142_1387+144del	ENSP00000404372.2:n.1387+142_1387+144del
ENST00000524552.5:c.295+7_295+9del	ENSP00000435908.1:n.295+7_295+9del
ENST00000526110.5:c.1465+7_1465+9del	ENSP00000433584.1:n.1465+7_1465+9del
ENST00000526686.1:c.178+7_178+9del	ENSP00000435019.1:n.178+7_178+9del
ENST00000532091.1:n.1504_1506del
ENST00000532636.5:c.1522+7_1522+9del	ENSP00000437125.1:n.1522+7_1522+9del
ENST00000533540.5:c.1084+7_1084+9del	ENSP00000437189.1:n.1084+7_1084+9del
ENST00000534319.5:c.814+7_814+9del	ENSP00000433316.1:n.814+7_814+9del
ENST00000534624.5:c.1522+7_1522+9del	ENSP00000432083.1:n.1522+7_1522+9del
NM_006597.5:c.1522+7_1522+9del	NP_006588.1:n.1522+7_1522+9del
NM_153201.3:c.1387+142_1387+144del	NP_694881.1:n.1387+142_1387+144del
XM_011542798.1:c.1522+7_1522+9del	XP_011541100.1:n.1522+7_1522+9del
NM_006597.6:c.1522+7_1522+9del MANE Select	NP_006588.1:n.1522+7_1522+9del
NM_153201.4:c.1387+142_1387+144del	NP_694881.1:n.1387+142_1387+144del