Canonical Allele Identifier: CA2005597151
Gene: HSPA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059240_123059241delinsGA , CM000673.2:g.123059240_123059241delinsGA GRCh38
NC_000011.9:g.122929948_122929949delinsGA , CM000673.1:g.122929948_122929949delinsGA GRCh37
NC_000011.8:g.122435158_122435159delinsGA NCBI36
NG_029473.1:g.7896_7897delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1141_1142delinsTC MANE Select ENSP00000432083.1:p.Ser381=
ENST00000227378.7:c.1141_1142delinsTC ENSP00000227378.3:p.Ser381=
ENST00000453788.6:c.1141_1142delinsTC ENSP00000404372.2:p.Ser381=
ENST00000524552.5:c.-87_-86delinsTC ENSP00000435908.1:n.-87_-86delinsTC
ENST00000526110.5:c.1084_1085delinsTC ENSP00000433584.1:p.Ser362=
ENST00000526862.1:n.419_420delinsTC
ENST00000527983.5:n.1501_1502delinsTC
ENST00000532091.1:n.888_889delinsTC
ENST00000532636.5:c.1141_1142delinsTC ENSP00000437125.1:p.Ser381=
ENST00000533238.5:n.381-138_381-137delinsTC
ENST00000533540.5:c.703_704delinsTC ENSP00000437189.1:p.Ser235=
ENST00000534319.5:c.433_434delinsTC ENSP00000433316.1:p.Ser145=
ENST00000534624.5:c.1141_1142delinsTC ENSP00000432083.1:p.Ser381=
NM_006597.5:c.1141_1142delinsTC NP_006588.1:p.Ser381=
NM_153201.3:c.1141_1142delinsTC NP_694881.1:p.Ser381=
XM_011542798.1:c.1141_1142delinsTC XP_011541100.1:p.Ser381=
NM_006597.6:c.1141_1142delinsTC MANE Select NP_006588.1:p.Ser381=
NM_153201.4:c.1141_1142delinsTC NP_694881.1:p.Ser381=