Canonical Allele Identifier: CA2793937032
Gene: HSPA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058850_123058851insCCAAACACACCCAACAC , CM000673.2:g.123058850_123058851insCCAAACACACCCAACAC GRCh38
NC_000011.9:g.122929558_122929559insCCAAACACACCCAACAC , CM000673.1:g.122929558_122929559insCCAAACACACCCAACAC GRCh37
NC_000011.8:g.122434768_122434769insCCAAACACACCCAACAC NCBI36
NG_029473.1:g.8286_8287insGTGTTGGGTGTGTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG MANE Select ENSP00000432083.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
ENST00000227378.7:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG ENSP00000227378.3:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
ENST00000453788.6:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG ENSP00000404372.2:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
ENST00000524552.5:c.97-21_97-20insGTGTTGGGTGTGTTTGG ENSP00000435908.1:n.97-21_97-20insGTGTTGGGTGTGTTTGG
ENST00000526110.5:c.1267-21_1267-20insGTGTTGGGTGTGTTTGG ENSP00000433584.1:n.1267-21_1267-20insGTGTTGGGTGTGTTTGG
ENST00000526686.1:c.-42_-41insGTGTTGGGTGTGTTTGG ENSP00000435019.1:n.-42_-41insGTGTTGGGTGTGTTTGG
ENST00000532091.1:n.1278_1279insGTGTTGGGTGTGTTTGG
ENST00000532636.5:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG ENSP00000437125.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
ENST00000533238.5:n.426-21_426-20insGTGTTGGGTGTGTTTGG
ENST00000533540.5:c.886-21_886-20insGTGTTGGGTGTGTTTGG ENSP00000437189.1:n.886-21_886-20insGTGTTGGGTGTGTTTGG
ENST00000534319.5:c.616-21_616-20insGTGTTGGGTGTGTTTGG ENSP00000433316.1:n.616-21_616-20insGTGTTGGGTGTGTTTGG
ENST00000534624.5:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG ENSP00000432083.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
NM_006597.5:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG NP_006588.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
NM_153201.3:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG NP_694881.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
XM_011542798.1:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG XP_011541100.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
NM_006597.6:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG MANE Select NP_006588.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG
NM_153201.4:c.1324-21_1324-20insGTGTTGGGTGTGTTTGG NP_694881.1:n.1324-21_1324-20insGTGTTGGGTGTGTTTGG