Canonical Allele Identifier: CA2545445323

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058572_123058574dup , CM000673.2:g.123058572_123058574dup	GRCh38
NC_000011.9:g.122929280_122929282dup , CM000673.1:g.122929280_122929282dup	GRCh37
NC_000011.8:g.122434490_122434492dup	NCBI36
NG_029473.1:g.8565_8567dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+60_1522+62dup MANE Select	ENSP00000432083.1:n.1522+60_1522+62dup
ENST00000227378.7:c.1522+60_1522+62dup	ENSP00000227378.3:n.1522+60_1522+62dup
ENST00000453788.6:c.1387+195_1387+197dup	ENSP00000404372.2:n.1387+195_1387+197dup
ENST00000524552.5:c.295+60_295+62dup	ENSP00000435908.1:n.295+60_295+62dup
ENST00000526110.5:c.1465+60_1465+62dup	ENSP00000433584.1:n.1465+60_1465+62dup
ENST00000526686.1:c.178+60_178+62dup	ENSP00000435019.1:n.178+60_178+62dup
ENST00000532091.1:n.1557_1559dup
ENST00000532636.5:c.1522+60_1522+62dup	ENSP00000437125.1:n.1522+60_1522+62dup
ENST00000533540.5:c.1084+60_1084+62dup	ENSP00000437189.1:n.1084+60_1084+62dup
ENST00000534319.5:c.814+60_814+62dup	ENSP00000433316.1:n.814+60_814+62dup
ENST00000534624.5:c.1522+60_1522+62dup	ENSP00000432083.1:n.1522+60_1522+62dup
NM_006597.5:c.1522+60_1522+62dup	NP_006588.1:n.1522+60_1522+62dup
NM_153201.3:c.1387+195_1387+197dup	NP_694881.1:n.1387+195_1387+197dup
XM_011542798.1:c.1522+60_1522+62dup	XP_011541100.1:n.1522+60_1522+62dup
NM_006597.6:c.1522+60_1522+62dup MANE Select	NP_006588.1:n.1522+60_1522+62dup
NM_153201.4:c.1387+195_1387+197dup	NP_694881.1:n.1387+195_1387+197dup