Canonical Allele Identifier: CA2681649736
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528837_5528839del , CM000669.2:g.5528837_5528839del GRCh38
NC_000007.13:g.5568468_5568470del , CM000669.1:g.5568468_5568470del GRCh37
NC_000007.12:g.5534994_5534996del NCBI36
NG_007992.1:g.6764_6766del , LRG_132:g.6764_6766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-119_364-117del ENSP00000407473.2:n.364-119_364-117del
ENST00000473257.3:c.235-119_235-117del ENSP00000501773.1:n.235-119_235-117del
ENST00000477812.2:n.792_794del
ENST00000484841.6:n.559-119_559-117del
ENST00000493945.6:c.364-119_364-117del ENSP00000494269.1:n.364-119_364-117del
ENST00000642480.2:c.364-119_364-117del ENSP00000495995.2:n.364-119_364-117del
ENST00000645576.1:c.364-167_364-165del ENSP00000496101.1:n.364-167_364-165del
ENST00000646664.1:c.364-119_364-117del MANE Select ENSP00000494750.1:n.364-119_364-117del
ENST00000647275.1:c.-3-119_-3-117del ENSP00000494185.1:n.-3-119_-3-117del
ENST00000674681.1:c.364-119_364-117del ENSP00000502821.1:n.364-119_364-117del
ENST00000675515.1:c.364-119_364-117del ENSP00000501862.1:n.364-119_364-117del
ENST00000676189.1:c.375-131_375-129del ENSP00000502538.1:n.375-131_375-129del
ENST00000676319.1:c.87+733_87+735del ENSP00000502193.1:n.87+733_87+735del
ENST00000676397.1:c.364-119_364-117del ENSP00000502286.1:n.364-119_364-117del
ENST00000331789.9:c.364-119_364-117del ENSP00000349960.4:n.364-119_364-117del
ENST00000425660.5:c.*27-119_*27-117del ENSP00000409264.1:n.*27-119_*27-117del
ENST00000432588.5:c.364-119_364-117del ENSP00000407473.1:n.364-119_364-117del
ENST00000462494.5:n.770_772del
ENST00000473257.1:n.82-119_82-117del
ENST00000477812.1:n.571-119_571-117del
ENST00000484841.5:n.519-119_519-117del
ENST00000493945.5:n.370-119_370-117del
NM_001101.3:c.364-119_364-117del , LRG_132t1:c.364-119_364-117del NP_001092.1:n.364-119_364-117del
XM_006715764.1:c.-122_-120del XP_006715827.1:n.-122_-120del
NM_001101.4:c.364-119_364-117del NP_001092.1:n.364-119_364-117del
NM_001101.5:c.364-119_364-117del MANE Select NP_001092.1:n.364-119_364-117del