Canonical Allele Identifier: CA1097928575
Gene: ACTB HGNC NCBI

Linked Data

dbSNP Id: rs1784817099
gnomAD v3: 7-5528734-T-TA
gnomAD v4: 7-5528734-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528735dup , CM000669.2:g.5528735dup GRCh38
NC_000007.13:g.5568366dup , CM000669.1:g.5568366dup GRCh37
NC_000007.12:g.5534892dup NCBI36
NG_007992.1:g.6867dup , LRG_132:g.6867dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-16dup ENSP00000407473.2:n.364-16dup
ENST00000473257.3:c.235-16dup ENSP00000501773.1:n.235-16dup
ENST00000477812.2:n.895dup
ENST00000484841.6:n.559-16dup
ENST00000493945.6:c.364-16dup ENSP00000494269.1:n.364-16dup
ENST00000642480.2:c.364-16dup ENSP00000495995.2:n.364-16dup
ENST00000645576.1:c.364-64dup ENSP00000496101.1:n.364-64dup
ENST00000646664.1:c.364-16dup MANE Select ENSP00000494750.1:n.364-16dup
ENST00000647275.1:c.-3-16dup ENSP00000494185.1:n.-3-16dup
ENST00000674681.1:c.364-16dup ENSP00000502821.1:n.364-16dup
ENST00000675515.1:c.364-16dup ENSP00000501862.1:n.364-16dup
ENST00000676189.1:c.375-28dup ENSP00000502538.1:n.375-28dup
ENST00000676319.1:c.87+836dup ENSP00000502193.1:n.87+836dup
ENST00000676397.1:c.364-16dup ENSP00000502286.1:n.364-16dup
ENST00000331789.9:c.364-16dup ENSP00000349960.4:n.364-16dup
ENST00000425660.5:c.*27-16dup ENSP00000409264.1:n.*27-16dup
ENST00000432588.5:c.364-16dup ENSP00000407473.1:n.364-16dup
ENST00000462494.5:n.873dup
ENST00000473257.1:n.82-16dup
ENST00000477812.1:n.571-16dup
ENST00000484841.5:n.519-16dup
ENST00000493945.5:n.370-16dup
NM_001101.3:c.364-16dup , LRG_132t1:c.364-16dup NP_001092.1:n.364-16dup
XM_006715764.1:c.-19dup XP_006715827.1:n.-19dup
NM_001101.4:c.364-16dup NP_001092.1:n.364-16dup
NM_001101.5:c.364-16dup MANE Select NP_001092.1:n.364-16dup