Canonical Allele Identifier: CA2005597302

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059278_123059281delinsTAAC , CM000673.2:g.123059278_123059281delinsTAAC	GRCh38
NC_000011.9:g.122929986_122929989delinsTAAC , CM000673.1:g.122929986_122929989delinsTAAC	GRCh37
NC_000011.8:g.122435196_122435199delinsTAAC	NCBI36
NG_029473.1:g.7856_7859delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-20_1121-17delinsGTTA MANE Select	ENSP00000432083.1:n.1121-20_1121-17delinsGTTA
ENST00000227378.7:c.1121-20_1121-17delinsGTTA	ENSP00000227378.3:n.1121-20_1121-17delinsGTTA
ENST00000453788.6:c.1121-20_1121-17delinsGTTA	ENSP00000404372.2:n.1121-20_1121-17delinsGTTA
ENST00000524552.5:c.-127_-124delinsGTTA	ENSP00000435908.1:n.-127_-124delinsGTTA
ENST00000526110.5:c.1064-20_1064-17delinsGTTA	ENSP00000433584.1:n.1064-20_1064-17delinsGTTA
ENST00000526862.1:n.399-20_399-17delinsGTTA
ENST00000527983.5:n.1461_1464delinsGTTA
ENST00000532091.1:n.868-20_868-17delinsGTTA
ENST00000532636.5:c.1121-20_1121-17delinsGTTA	ENSP00000437125.1:n.1121-20_1121-17delinsGTTA
ENST00000533238.5:n.381-178_381-175delinsGTTA
ENST00000533540.5:c.683-20_683-17delinsGTTA	ENSP00000437189.1:n.683-20_683-17delinsGTTA
ENST00000534319.5:c.413-20_413-17delinsGTTA	ENSP00000433316.1:n.413-20_413-17delinsGTTA
ENST00000534624.5:c.1121-20_1121-17delinsGTTA	ENSP00000432083.1:n.1121-20_1121-17delinsGTTA
NM_006597.5:c.1121-20_1121-17delinsGTTA	NP_006588.1:n.1121-20_1121-17delinsGTTA
NM_153201.3:c.1121-20_1121-17delinsGTTA	NP_694881.1:n.1121-20_1121-17delinsGTTA
XM_011542798.1:c.1121-20_1121-17delinsGTTA	XP_011541100.1:n.1121-20_1121-17delinsGTTA
NM_006597.6:c.1121-20_1121-17delinsGTTA MANE Select	NP_006588.1:n.1121-20_1121-17delinsGTTA
NM_153201.4:c.1121-20_1121-17delinsGTTA	NP_694881.1:n.1121-20_1121-17delinsGTTA