Canonical Allele Identifier: CA2509119897

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059281_123059283del , CM000673.2:g.123059281_123059283del	GRCh38
NC_000011.9:g.122929989_122929991del , CM000673.1:g.122929989_122929991del	GRCh37
NC_000011.8:g.122435199_122435201del	NCBI36
NG_029473.1:g.7854_7856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-22_1121-20del MANE Select	ENSP00000432083.1:n.1121-22_1121-20del
ENST00000227378.7:c.1121-22_1121-20del	ENSP00000227378.3:n.1121-22_1121-20del
ENST00000453788.6:c.1121-22_1121-20del	ENSP00000404372.2:n.1121-22_1121-20del
ENST00000524552.5:c.-129_-127del	ENSP00000435908.1:n.-129_-127del
ENST00000526110.5:c.1064-22_1064-20del	ENSP00000433584.1:n.1064-22_1064-20del
ENST00000526862.1:n.399-22_399-20del
ENST00000527983.5:n.1459_1461del
ENST00000532091.1:n.868-22_868-20del
ENST00000532636.5:c.1121-22_1121-20del	ENSP00000437125.1:n.1121-22_1121-20del
ENST00000533238.5:n.381-180_381-178del
ENST00000533540.5:c.683-22_683-20del	ENSP00000437189.1:n.683-22_683-20del
ENST00000534319.5:c.413-22_413-20del	ENSP00000433316.1:n.413-22_413-20del
ENST00000534624.5:c.1121-22_1121-20del	ENSP00000432083.1:n.1121-22_1121-20del
NM_006597.5:c.1121-22_1121-20del	NP_006588.1:n.1121-22_1121-20del
NM_153201.3:c.1121-22_1121-20del	NP_694881.1:n.1121-22_1121-20del
XM_011542798.1:c.1121-22_1121-20del	XP_011541100.1:n.1121-22_1121-20del
NM_006597.6:c.1121-22_1121-20del MANE Select	NP_006588.1:n.1121-22_1121-20del
NM_153201.4:c.1121-22_1121-20del	NP_694881.1:n.1121-22_1121-20del