Canonical Allele Identifier: CA2005597323
Gene: HSPA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059284_123059286delinsTAA , CM000673.2:g.123059284_123059286delinsTAA GRCh38
NC_000011.9:g.122929992_122929994delinsTAA , CM000673.1:g.122929992_122929994delinsTAA GRCh37
NC_000011.8:g.122435202_122435204delinsTAA NCBI36
NG_029473.1:g.7851_7853delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1121-25_1121-23delinsTTA MANE Select ENSP00000432083.1:n.1121-25_1121-23delinsTTA
ENST00000227378.7:c.1121-25_1121-23delinsTTA ENSP00000227378.3:n.1121-25_1121-23delinsTTA
ENST00000453788.6:c.1121-25_1121-23delinsTTA ENSP00000404372.2:n.1121-25_1121-23delinsTTA
ENST00000524552.5:c.-132_-130delinsTTA ENSP00000435908.1:n.-132_-130delinsTTA
ENST00000526110.5:c.1064-25_1064-23delinsTTA ENSP00000433584.1:n.1064-25_1064-23delinsTTA
ENST00000526862.1:n.399-25_399-23delinsTTA
ENST00000527983.5:n.1456_1458delinsTTA
ENST00000532091.1:n.868-25_868-23delinsTTA
ENST00000532636.5:c.1121-25_1121-23delinsTTA ENSP00000437125.1:n.1121-25_1121-23delinsTTA
ENST00000533238.5:n.381-183_381-181delinsTTA
ENST00000533540.5:c.683-25_683-23delinsTTA ENSP00000437189.1:n.683-25_683-23delinsTTA
ENST00000534319.5:c.413-25_413-23delinsTTA ENSP00000433316.1:n.413-25_413-23delinsTTA
ENST00000534624.5:c.1121-25_1121-23delinsTTA ENSP00000432083.1:n.1121-25_1121-23delinsTTA
NM_006597.5:c.1121-25_1121-23delinsTTA NP_006588.1:n.1121-25_1121-23delinsTTA
NM_153201.3:c.1121-25_1121-23delinsTTA NP_694881.1:n.1121-25_1121-23delinsTTA
XM_011542798.1:c.1121-25_1121-23delinsTTA XP_011541100.1:n.1121-25_1121-23delinsTTA
NM_006597.6:c.1121-25_1121-23delinsTTA MANE Select NP_006588.1:n.1121-25_1121-23delinsTTA
NM_153201.4:c.1121-25_1121-23delinsTTA NP_694881.1:n.1121-25_1121-23delinsTTA