Canonical Allele Identifier: CA2578822279
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528927_5528928del , CM000669.2:g.5528927_5528928del GRCh38
NC_000007.13:g.5568558_5568559del , CM000669.1:g.5568558_5568559del GRCh37
NC_000007.12:g.5535084_5535085del NCBI36
NG_007992.1:g.6676_6677del , LRG_132:g.6676_6677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-207_364-206del ENSP00000407473.2:n.364-207_364-206del
ENST00000473257.3:c.235-207_235-206del ENSP00000501773.1:n.235-207_235-206del
ENST00000477812.2:n.704_705del
ENST00000484841.6:n.558+93_558+94del
ENST00000493945.6:c.364-207_364-206del ENSP00000494269.1:n.364-207_364-206del
ENST00000642480.2:c.364-207_364-206del ENSP00000495995.2:n.364-207_364-206del
ENST00000645576.1:c.363+235_363+236del ENSP00000496101.1:n.363+235_363+236del
ENST00000646664.1:c.364-207_364-206del MANE Select ENSP00000494750.1:n.364-207_364-206del
ENST00000647275.1:c.-3-207_-3-206del ENSP00000494185.1:n.-3-207_-3-206del
ENST00000674681.1:c.364-207_364-206del ENSP00000502821.1:n.364-207_364-206del
ENST00000675515.1:c.364-207_364-206del ENSP00000501862.1:n.364-207_364-206del
ENST00000676189.1:c.375-219_375-218del ENSP00000502538.1:n.375-219_375-218del
ENST00000676319.1:c.87+645_87+646del ENSP00000502193.1:n.87+645_87+646del
ENST00000676397.1:c.364-207_364-206del ENSP00000502286.1:n.364-207_364-206del
ENST00000331789.9:c.364-207_364-206del ENSP00000349960.4:n.364-207_364-206del
ENST00000425660.5:c.*26+93_*26+94del ENSP00000409264.1:n.*26+93_*26+94del
ENST00000432588.5:c.364-207_364-206del ENSP00000407473.1:n.364-207_364-206del
ENST00000462494.5:n.682_683del
ENST00000473257.1:n.82-207_82-206del
ENST00000477812.1:n.571-207_571-206del
ENST00000484841.5:n.519-207_519-206del
ENST00000493945.5:n.370-207_370-206del
NM_001101.3:c.364-207_364-206del , LRG_132t1:c.364-207_364-206del NP_001092.1:n.364-207_364-206del
XM_006715764.1:c.-210_-209del XP_006715827.1:n.-210_-209del
NM_001101.4:c.364-207_364-206del NP_001092.1:n.364-207_364-206del
NM_001101.5:c.364-207_364-206del MANE Select NP_001092.1:n.364-207_364-206del