Canonical Allele Identifier: CA2572114351

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059319_123059323del , CM000673.2:g.123059319_123059323del	GRCh38
NC_000011.9:g.122930027_122930031del , CM000673.1:g.122930027_122930031del	GRCh37
NC_000011.8:g.122435237_122435241del	NCBI36
NG_029473.1:g.7814_7818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-62_1121-58del MANE Select	ENSP00000432083.1:n.1121-62_1121-58del
ENST00000227378.7:c.1121-62_1121-58del	ENSP00000227378.3:n.1121-62_1121-58del
ENST00000453788.6:c.1121-62_1121-58del	ENSP00000404372.2:n.1121-62_1121-58del
ENST00000524552.5:c.-169_-165del	ENSP00000435908.1:n.-169_-165del
ENST00000526110.5:c.1064-62_1064-58del	ENSP00000433584.1:n.1064-62_1064-58del
ENST00000526862.1:n.399-62_399-58del
ENST00000527983.5:n.1419_1423del
ENST00000532091.1:n.868-62_868-58del
ENST00000532636.5:c.1121-62_1121-58del	ENSP00000437125.1:n.1121-62_1121-58del
ENST00000533238.5:n.381-220_381-216del
ENST00000533540.5:c.683-62_683-58del	ENSP00000437189.1:n.683-62_683-58del
ENST00000534319.5:c.413-62_413-58del	ENSP00000433316.1:n.413-62_413-58del
ENST00000534624.5:c.1121-62_1121-58del	ENSP00000432083.1:n.1121-62_1121-58del
NM_006597.5:c.1121-62_1121-58del	NP_006588.1:n.1121-62_1121-58del
NM_153201.3:c.1121-62_1121-58del	NP_694881.1:n.1121-62_1121-58del
XM_011542798.1:c.1121-62_1121-58del	XP_011541100.1:n.1121-62_1121-58del
NM_006597.6:c.1121-62_1121-58del MANE Select	NP_006588.1:n.1121-62_1121-58del
NM_153201.4:c.1121-62_1121-58del	NP_694881.1:n.1121-62_1121-58del