Canonical Allele Identifier: CA2616532915
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059318_123059320del , CM000673.2:g.123059318_123059320del GRCh38
NC_000011.9:g.122930026_122930028del , CM000673.1:g.122930026_122930028del GRCh37
NC_000011.8:g.122435236_122435238del NCBI36
NG_029473.1:g.7819_7821del

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1121-57_1121-55del MANE Select ENSP00000432083.1:n.1121-57_1121-55del
ENST00000227378.7:c.1121-57_1121-55del ENSP00000227378.3:n.1121-57_1121-55del
ENST00000453788.6:c.1121-57_1121-55del ENSP00000404372.2:n.1121-57_1121-55del
ENST00000524552.5:c.-164_-162del ENSP00000435908.1:n.-164_-162del
ENST00000526110.5:c.1064-57_1064-55del ENSP00000433584.1:n.1064-57_1064-55del
ENST00000526862.1:n.399-57_399-55del
ENST00000527983.5:n.1424_1426del
ENST00000532091.1:n.868-57_868-55del
ENST00000532636.5:c.1121-57_1121-55del ENSP00000437125.1:n.1121-57_1121-55del
ENST00000533238.5:n.381-215_381-213del
ENST00000533540.5:c.683-57_683-55del ENSP00000437189.1:n.683-57_683-55del
ENST00000534319.5:c.413-57_413-55del ENSP00000433316.1:n.413-57_413-55del
ENST00000534624.5:c.1121-57_1121-55del ENSP00000432083.1:n.1121-57_1121-55del
NM_006597.5:c.1121-57_1121-55del NP_006588.1:n.1121-57_1121-55del
NM_153201.3:c.1121-57_1121-55del NP_694881.1:n.1121-57_1121-55del
XM_011542798.1:c.1121-57_1121-55del XP_011541100.1:n.1121-57_1121-55del
NM_006597.6:c.1121-57_1121-55del MANE Select NP_006588.1:n.1121-57_1121-55del
NM_153201.4:c.1121-57_1121-55del NP_694881.1:n.1121-57_1121-55del