Canonical Allele Identifier: CA2681649860
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528956_5528957insAA , CM000669.2:g.5528956_5528957insAA GRCh38
NC_000007.13:g.5568587_5568588insAA , CM000669.1:g.5568587_5568588insAA GRCh37
NC_000007.12:g.5535113_5535114insAA NCBI36
NG_007992.1:g.6646_6647insTT , LRG_132:g.6646_6647insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.363+205_363+206insTT ENSP00000407473.2:n.363+205_363+206insTT
ENST00000473257.3:c.234+205_234+206insTT ENSP00000501773.1:n.234+205_234+206insTT
ENST00000477812.2:n.674_675insTT
ENST00000484841.6:n.558+63_558+64insTT
ENST00000493945.6:c.363+205_363+206insTT ENSP00000494269.1:n.363+205_363+206insTT
ENST00000642480.2:c.363+205_363+206insTT ENSP00000495995.2:n.363+205_363+206insTT
ENST00000645025.1:n.550_551insTT
ENST00000645576.1:c.363+205_363+206insTT ENSP00000496101.1:n.363+205_363+206insTT
ENST00000646664.1:c.363+205_363+206insTT MANE Select ENSP00000494750.1:n.363+205_363+206insTT
ENST00000647275.1:c.-3-237_-3-236insTT ENSP00000494185.1:n.-3-237_-3-236insTT
ENST00000674681.1:c.363+205_363+206insTT ENSP00000502821.1:n.363+205_363+206insTT
ENST00000675515.1:c.363+205_363+206insTT ENSP00000501862.1:n.363+205_363+206insTT
ENST00000676189.1:c.374+194_374+195insTT ENSP00000502538.1:n.374+194_374+195insTT
ENST00000676319.1:c.87+615_87+616insTT ENSP00000502193.1:n.87+615_87+616insTT
ENST00000676397.1:c.363+205_363+206insTT ENSP00000502286.1:n.363+205_363+206insTT
ENST00000331789.9:c.363+205_363+206insTT ENSP00000349960.4:n.363+205_363+206insTT
ENST00000425660.5:c.*26+63_*26+64insTT ENSP00000409264.1:n.*26+63_*26+64insTT
ENST00000432588.5:c.363+205_363+206insTT ENSP00000407473.1:n.363+205_363+206insTT
ENST00000462494.5:n.652_653insTT
ENST00000473257.1:n.82-237_82-236insTT
ENST00000477812.1:n.570+205_570+206insTT
ENST00000484841.5:n.518+205_518+206insTT
ENST00000493945.5:n.369+205_369+206insTT
NM_001101.3:c.363+205_363+206insTT , LRG_132t1:c.363+205_363+206insTT NP_001092.1:n.363+205_363+206insTT
XM_006715764.1:c.-240_-239insTT XP_006715827.1:n.-240_-239insTT
NM_001101.4:c.363+205_363+206insTT NP_001092.1:n.363+205_363+206insTT
NM_001101.5:c.363+205_363+206insTT MANE Select NP_001092.1:n.363+205_363+206insTT