Canonical Allele Identifier: CA2681649800
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528886_5528889dup , CM000669.2:g.5528886_5528889dup GRCh38
NC_000007.13:g.5568517_5568520dup , CM000669.1:g.5568517_5568520dup GRCh37
NC_000007.12:g.5535043_5535046dup NCBI36
NG_007992.1:g.6713_6716dup , LRG_132:g.6713_6716dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-170_364-167dup ENSP00000407473.2:n.364-170_364-167dup
ENST00000473257.3:c.235-170_235-167dup ENSP00000501773.1:n.235-170_235-167dup
ENST00000477812.2:n.741_744dup
ENST00000484841.6:n.558+130_558+133dup
ENST00000493945.6:c.364-170_364-167dup ENSP00000494269.1:n.364-170_364-167dup
ENST00000642480.2:c.364-170_364-167dup ENSP00000495995.2:n.364-170_364-167dup
ENST00000645576.1:c.364-218_364-215dup ENSP00000496101.1:n.364-218_364-215dup
ENST00000646664.1:c.364-170_364-167dup MANE Select ENSP00000494750.1:n.364-170_364-167dup
ENST00000647275.1:c.-3-170_-3-167dup ENSP00000494185.1:n.-3-170_-3-167dup
ENST00000674681.1:c.364-170_364-167dup ENSP00000502821.1:n.364-170_364-167dup
ENST00000675515.1:c.364-170_364-167dup ENSP00000501862.1:n.364-170_364-167dup
ENST00000676189.1:c.375-182_375-179dup ENSP00000502538.1:n.375-182_375-179dup
ENST00000676319.1:c.87+682_87+685dup ENSP00000502193.1:n.87+682_87+685dup
ENST00000676397.1:c.364-170_364-167dup ENSP00000502286.1:n.364-170_364-167dup
ENST00000331789.9:c.364-170_364-167dup ENSP00000349960.4:n.364-170_364-167dup
ENST00000425660.5:c.*26+130_*26+133dup ENSP00000409264.1:n.*26+130_*26+133dup
ENST00000432588.5:c.364-170_364-167dup ENSP00000407473.1:n.364-170_364-167dup
ENST00000462494.5:n.719_722dup
ENST00000473257.1:n.82-170_82-167dup
ENST00000477812.1:n.571-170_571-167dup
ENST00000484841.5:n.519-170_519-167dup
ENST00000493945.5:n.370-170_370-167dup
NM_001101.3:c.364-170_364-167dup , LRG_132t1:c.364-170_364-167dup NP_001092.1:n.364-170_364-167dup
XM_006715764.1:c.-173_-170dup XP_006715827.1:n.-173_-170dup
NM_001101.4:c.364-170_364-167dup NP_001092.1:n.364-170_364-167dup
NM_001101.5:c.364-170_364-167dup MANE Select NP_001092.1:n.364-170_364-167dup