Canonical Allele Identifier: CA2681649771
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528862_5528863insACACACCC , CM000669.2:g.5528862_5528863insACACACCC GRCh38
NC_000007.13:g.5568493_5568494insACACACCC , CM000669.1:g.5568493_5568494insACACACCC GRCh37
NC_000007.12:g.5535019_5535020insACACACCC NCBI36
NG_007992.1:g.6739_6740insGGGTGTGT , LRG_132:g.6739_6740insGGGTGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-144_364-143insGGGTGTGT ENSP00000407473.2:n.364-144_364-143insGGGTGTGT
ENST00000473257.3:c.235-144_235-143insGGGTGTGT ENSP00000501773.1:n.235-144_235-143insGGGTGTGT
ENST00000477812.2:n.767_768insGGGTGTGT
ENST00000484841.6:n.559-144_559-143insGGGTGTGT
ENST00000493945.6:c.364-144_364-143insGGGTGTGT ENSP00000494269.1:n.364-144_364-143insGGGTGTGT
ENST00000642480.2:c.364-144_364-143insGGGTGTGT ENSP00000495995.2:n.364-144_364-143insGGGTGTGT
ENST00000645576.1:c.364-192_364-191insGGGTGTGT ENSP00000496101.1:n.364-192_364-191insGGGTGTGT
ENST00000646664.1:c.364-144_364-143insGGGTGTGT MANE Select ENSP00000494750.1:n.364-144_364-143insGGGTGTGT
ENST00000647275.1:c.-3-144_-3-143insGGGTGTGT ENSP00000494185.1:n.-3-144_-3-143insGGGTGTGT
ENST00000674681.1:c.364-144_364-143insGGGTGTGT ENSP00000502821.1:n.364-144_364-143insGGGTGTGT
ENST00000675515.1:c.364-144_364-143insGGGTGTGT ENSP00000501862.1:n.364-144_364-143insGGGTGTGT
ENST00000676189.1:c.375-156_375-155insGGGTGTGT ENSP00000502538.1:n.375-156_375-155insGGGTGTGT
ENST00000676319.1:c.87+708_87+709insGGGTGTGT ENSP00000502193.1:n.87+708_87+709insGGGTGTGT
ENST00000676397.1:c.364-144_364-143insGGGTGTGT ENSP00000502286.1:n.364-144_364-143insGGGTGTGT
ENST00000331789.9:c.364-144_364-143insGGGTGTGT ENSP00000349960.4:n.364-144_364-143insGGGTGTGT
ENST00000425660.5:c.*27-144_*27-143insGGGTGTGT ENSP00000409264.1:n.*27-144_*27-143insGGGTGTGT
ENST00000432588.5:c.364-144_364-143insGGGTGTGT ENSP00000407473.1:n.364-144_364-143insGGGTGTGT
ENST00000462494.5:n.745_746insGGGTGTGT
ENST00000473257.1:n.82-144_82-143insGGGTGTGT
ENST00000477812.1:n.571-144_571-143insGGGTGTGT
ENST00000484841.5:n.519-144_519-143insGGGTGTGT
ENST00000493945.5:n.370-144_370-143insGGGTGTGT
NM_001101.3:c.364-144_364-143insGGGTGTGT , LRG_132t1:c.364-144_364-143insGGGTGTGT NP_001092.1:n.364-144_364-143insGGGTGTGT
XM_006715764.1:c.-147_-146insGGGTGTGT XP_006715827.1:n.-147_-146insGGGTGTGT
NM_001101.4:c.364-144_364-143insGGGTGTGT NP_001092.1:n.364-144_364-143insGGGTGTGT
NM_001101.5:c.364-144_364-143insGGGTGTGT MANE Select NP_001092.1:n.364-144_364-143insGGGTGTGT