Canonical Allele Identifier: CA383058330
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059166C>T , CM000673.2:g.123059166C>T GRCh38
NC_000011.9:g.122929874C>T , CM000673.1:g.122929874C>T GRCh37
NC_000011.8:g.122435084C>T NCBI36
NG_029473.1:g.7971G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1216G>A MANE Select ENSP00000432083.1:p.Ala406Thr
ENST00000227378.7:c.1216G>A ENSP00000227378.3:p.Ala406Thr
ENST00000453788.6:c.1216G>A ENSP00000404372.2:p.Ala406Thr
ENST00000524552.5:c.-12G>A ENSP00000435908.1:n.-12G>A
ENST00000526110.5:c.1159G>A ENSP00000433584.1:p.Ala387Thr
ENST00000526862.1:n.494G>A
ENST00000532091.1:n.963G>A
ENST00000532636.5:c.1216G>A ENSP00000437125.1:p.Ala406Thr
ENST00000533238.5:n.381-63G>A
ENST00000533540.5:c.778G>A ENSP00000437189.1:p.Ala260Thr
ENST00000534319.5:c.508G>A ENSP00000433316.1:p.Ala170Thr
ENST00000534624.5:c.1216G>A ENSP00000432083.1:p.Ala406Thr
NM_006597.5:c.1216G>A NP_006588.1:p.Ala406Thr
NM_153201.3:c.1216G>A NP_694881.1:p.Ala406Thr
XM_011542798.1:c.1216G>A XP_011541100.1:p.Ala406Thr
NM_006597.6:c.1216G>A MANE Select NP_006588.1:p.Ala406Thr
NM_153201.4:c.1216G>A NP_694881.1:p.Ala406Thr