Canonical Allele Identifier: CA383058152
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059126G>C , CM000673.2:g.123059126G>C GRCh38
NC_000011.9:g.122929834G>C , CM000673.1:g.122929834G>C GRCh37
NC_000011.8:g.122435044G>C NCBI36
NG_029473.1:g.8011C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1256C>G MANE Select ENSP00000432083.1:p.Thr419Ser
ENST00000227378.7:c.1256C>G ENSP00000227378.3:p.Thr419Ser
ENST00000453788.6:c.1256C>G ENSP00000404372.2:p.Thr419Ser
ENST00000524552.5:c.29C>G ENSP00000435908.1:p.Thr10Ser
ENST00000526110.5:c.1199C>G ENSP00000433584.1:p.Thr400Ser
ENST00000532091.1:n.1003C>G
ENST00000532636.5:c.1256C>G ENSP00000437125.1:p.Thr419Ser
ENST00000533238.5:n.381-23C>G
ENST00000533540.5:c.818C>G ENSP00000437189.1:p.Thr273Ser
ENST00000534319.5:c.548C>G ENSP00000433316.1:p.Thr183Ser
ENST00000534624.5:c.1256C>G ENSP00000432083.1:p.Thr419Ser
NM_006597.5:c.1256C>G NP_006588.1:p.Thr419Ser
NM_153201.3:c.1256C>G NP_694881.1:p.Thr419Ser
XM_011542798.1:c.1256C>G XP_011541100.1:p.Thr419Ser
NM_006597.6:c.1256C>G MANE Select NP_006588.1:p.Thr419Ser
NM_153201.4:c.1256C>G NP_694881.1:p.Thr419Ser