Canonical Allele Identifier: CA2616532797
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058832_123058833insGAATAAGCACACCAGGCTGGTTGTCAGAATAGGTAGTGAAGGTCTGTGTCTGCT , CM000673.2:g.123058832_123058833insGAATAAGCACACCAGGCTGGTTGTCAGAATAGGTAGTGAAGGTCTGTGTCTGCT GRCh38
NC_000011.9:g.122929540_122929541insGAATAAGCACACCAGGCTGGTTGTCAGAATAGGTAGTGAAGGTCTGTGTCTGCT , CM000673.1:g.122929540_122929541insGAATAAGCACACCAGGCTGGTTGTCAGAATAGGTAGTGAAGGTCTGTGTCTGCT GRCh37
NC_000011.8:g.122434750_122434751insGAATAAGCACACCAGGCTGGTTGTCAGAATAGGTAGTGAAGGTCTGTGTCTGCT NCBI36
NG_029473.1:g.8306_8307insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG MANE Select ENSP00000432083.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCT...
ENST00000227378.7:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000227378.3:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCT...
ENST00000453788.6:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000404372.2:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCT...
ENST00000524552.5:c.97-1_97insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000435908.1:n.97-1_97insCAGACACAGACCTTCACTACCTATTCTGACA...
ENST00000526110.5:c.1267-1_1267insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000433584.1:n.1267-1_1267insCAGACACAGACCTTCACTACCTATTCT...
ENST00000526686.1:c.-22_-21insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000435019.1:n.-22_-21insCAGACACAGACCTTCACTACCTATTCTGACA...
ENST00000532091.1:n.1298_1299insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG
ENST00000532636.5:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000437125.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCT...
ENST00000533238.5:n.426-1_426insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG
ENST00000533540.5:c.886-1_886insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000437189.1:n.886-1_886insCAGACACAGACCTTCACTACCTATTCTGA...
ENST00000534319.5:c.616-1_616insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000433316.1:n.616-1_616insCAGACACAGACCTTCACTACCTATTCTGA...
ENST00000534624.5:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG ENSP00000432083.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCT...
NM_006597.5:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG NP_006588.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAAC...
NM_153201.3:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG NP_694881.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAAC...
XM_011542798.1:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG XP_011541100.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGAC...
NM_006597.6:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG MANE Select NP_006588.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAAC...
NM_153201.4:c.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAACCAGCCTGGTGTGCTTATTCAG NP_694881.1:n.1324-1_1324insCAGACACAGACCTTCACTACCTATTCTGACAAC...