Canonical Allele Identifier: CA2005597238

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059265_123059269delinsGCAAA , CM000673.2:g.123059265_123059269delinsGCAAA	GRCh38
NC_000011.9:g.122929973_122929977delinsGCAAA , CM000673.1:g.122929973_122929977delinsGCAAA	GRCh37
NC_000011.8:g.122435183_122435187delinsGCAAA	NCBI36
NG_029473.1:g.7868_7872delinsTTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-8_1121-4delinsTTTGC MANE Select	ENSP00000432083.1:n.1121-8_1121-4delinsTTTGC
ENST00000227378.7:c.1121-8_1121-4delinsTTTGC	ENSP00000227378.3:n.1121-8_1121-4delinsTTTGC
ENST00000453788.6:c.1121-8_1121-4delinsTTTGC	ENSP00000404372.2:n.1121-8_1121-4delinsTTTGC
ENST00000524552.5:c.-115_-111delinsTTTGC	ENSP00000435908.1:n.-115_-111delinsTTTGC
ENST00000526110.5:c.1064-8_1064-4delinsTTTGC	ENSP00000433584.1:n.1064-8_1064-4delinsTTTGC
ENST00000526862.1:n.399-8_399-4delinsTTTGC
ENST00000527983.5:n.1473_1477delinsTTTGC
ENST00000532091.1:n.868-8_868-4delinsTTTGC
ENST00000532636.5:c.1121-8_1121-4delinsTTTGC	ENSP00000437125.1:n.1121-8_1121-4delinsTTTGC
ENST00000533238.5:n.381-166_381-162delinsTTTGC
ENST00000533540.5:c.683-8_683-4delinsTTTGC	ENSP00000437189.1:n.683-8_683-4delinsTTTGC
ENST00000534319.5:c.413-8_413-4delinsTTTGC	ENSP00000433316.1:n.413-8_413-4delinsTTTGC
ENST00000534624.5:c.1121-8_1121-4delinsTTTGC	ENSP00000432083.1:n.1121-8_1121-4delinsTTTGC
NM_006597.5:c.1121-8_1121-4delinsTTTGC	NP_006588.1:n.1121-8_1121-4delinsTTTGC
NM_153201.3:c.1121-8_1121-4delinsTTTGC	NP_694881.1:n.1121-8_1121-4delinsTTTGC
XM_011542798.1:c.1121-8_1121-4delinsTTTGC	XP_011541100.1:n.1121-8_1121-4delinsTTTGC
NM_006597.6:c.1121-8_1121-4delinsTTTGC MANE Select	NP_006588.1:n.1121-8_1121-4delinsTTTGC
NM_153201.4:c.1121-8_1121-4delinsTTTGC	NP_694881.1:n.1121-8_1121-4delinsTTTGC