Canonical Allele Identifier: CA2681649819
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528901_5528906dup , CM000669.2:g.5528901_5528906dup GRCh38
NC_000007.13:g.5568532_5568537dup , CM000669.1:g.5568532_5568537dup GRCh37
NC_000007.12:g.5535058_5535063dup NCBI36
NG_007992.1:g.6696_6701dup , LRG_132:g.6696_6701dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-187_364-182dup ENSP00000407473.2:n.364-187_364-182dup
ENST00000473257.3:c.235-187_235-182dup ENSP00000501773.1:n.235-187_235-182dup
ENST00000477812.2:n.724_729dup
ENST00000484841.6:n.558+113_558+118dup
ENST00000493945.6:c.364-187_364-182dup ENSP00000494269.1:n.364-187_364-182dup
ENST00000642480.2:c.364-187_364-182dup ENSP00000495995.2:n.364-187_364-182dup
ENST00000645576.1:c.364-235_364-230dup ENSP00000496101.1:n.364-235_364-230dup
ENST00000646664.1:c.364-187_364-182dup MANE Select ENSP00000494750.1:n.364-187_364-182dup
ENST00000647275.1:c.-3-187_-3-182dup ENSP00000494185.1:n.-3-187_-3-182dup
ENST00000674681.1:c.364-187_364-182dup ENSP00000502821.1:n.364-187_364-182dup
ENST00000675515.1:c.364-187_364-182dup ENSP00000501862.1:n.364-187_364-182dup
ENST00000676189.1:c.375-199_375-194dup ENSP00000502538.1:n.375-199_375-194dup
ENST00000676319.1:c.87+665_87+670dup ENSP00000502193.1:n.87+665_87+670dup
ENST00000676397.1:c.364-187_364-182dup ENSP00000502286.1:n.364-187_364-182dup
ENST00000331789.9:c.364-187_364-182dup ENSP00000349960.4:n.364-187_364-182dup
ENST00000425660.5:c.*26+113_*26+118dup ENSP00000409264.1:n.*26+113_*26+118dup
ENST00000432588.5:c.364-187_364-182dup ENSP00000407473.1:n.364-187_364-182dup
ENST00000462494.5:n.702_707dup
ENST00000473257.1:n.82-187_82-182dup
ENST00000477812.1:n.571-187_571-182dup
ENST00000484841.5:n.519-187_519-182dup
ENST00000493945.5:n.370-187_370-182dup
NM_001101.3:c.364-187_364-182dup , LRG_132t1:c.364-187_364-182dup NP_001092.1:n.364-187_364-182dup
XM_006715764.1:c.-190_-185dup XP_006715827.1:n.-190_-185dup
NM_001101.4:c.364-187_364-182dup NP_001092.1:n.364-187_364-182dup
NM_001101.5:c.364-187_364-182dup MANE Select NP_001092.1:n.364-187_364-182dup