Canonical Allele Identifier: CA2580076752
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 2070531
ClinVar RCV Id: RCV002971221

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528734_5528735delinsCG , CM000669.2:g.5528734_5528735delinsCG GRCh38
NC_000007.13:g.5568365_5568366delinsCG , CM000669.1:g.5568365_5568366delinsCG GRCh37
NC_000007.12:g.5534891_5534892delinsCG NCBI36
NG_007992.1:g.6867_6868delinsCG , LRG_132:g.6867_6868delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-16_364-15delinsCG ENSP00000407473.2:n.364-16_364-15delinsCG
ENST00000473257.3:c.235-16_235-15delinsCG ENSP00000501773.1:n.235-16_235-15delinsCG
ENST00000477812.2:n.895_896delinsCG
ENST00000484841.6:n.559-16_559-15delinsCG
ENST00000493945.6:c.364-16_364-15delinsCG ENSP00000494269.1:n.364-16_364-15delinsCG
ENST00000642480.2:c.364-16_364-15delinsCG ENSP00000495995.2:n.364-16_364-15delinsCG
ENST00000645576.1:c.364-64_364-63delinsCG ENSP00000496101.1:n.364-64_364-63delinsCG
ENST00000646664.1:c.364-16_364-15delinsCG MANE Select ENSP00000494750.1:n.364-16_364-15delinsCG
ENST00000647275.1:c.-3-16_-3-15delinsCG ENSP00000494185.1:n.-3-16_-3-15delinsCG
ENST00000674681.1:c.364-16_364-15delinsCG ENSP00000502821.1:n.364-16_364-15delinsCG
ENST00000675515.1:c.364-16_364-15delinsCG ENSP00000501862.1:n.364-16_364-15delinsCG
ENST00000676189.1:c.375-28_375-27delinsCG ENSP00000502538.1:n.375-28_375-27delinsCG
ENST00000676319.1:c.87+836_87+837delinsCG ENSP00000502193.1:n.87+836_87+837delinsCG
ENST00000676397.1:c.364-16_364-15delinsCG ENSP00000502286.1:n.364-16_364-15delinsCG
ENST00000331789.9:c.364-16_364-15delinsCG ENSP00000349960.4:n.364-16_364-15delinsCG
ENST00000425660.5:c.*27-16_*27-15delinsCG ENSP00000409264.1:n.*27-16_*27-15delinsCG
ENST00000432588.5:c.364-16_364-15delinsCG ENSP00000407473.1:n.364-16_364-15delinsCG
ENST00000462494.5:n.873_874delinsCG
ENST00000473257.1:n.82-16_82-15delinsCG
ENST00000477812.1:n.571-16_571-15delinsCG
ENST00000484841.5:n.519-16_519-15delinsCG
ENST00000493945.5:n.370-16_370-15delinsCG
NM_001101.3:c.364-16_364-15delinsCG , LRG_132t1:c.364-16_364-15delinsCG NP_001092.1:n.364-16_364-15delinsCG
XM_006715764.1:c.-19_-18delinsCG XP_006715827.1:n.-19_-18delinsCG
NM_001101.4:c.364-16_364-15delinsCG NP_001092.1:n.364-16_364-15delinsCG
NM_001101.5:c.364-16_364-15delinsCG MANE Select NP_001092.1:n.364-16_364-15delinsCG