Canonical Allele Identifier: CA2580076753
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 2056508
ClinVar RCV Id: RCV002914621

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528735_5528736delinsGA , CM000669.2:g.5528735_5528736delinsGA GRCh38
NC_000007.13:g.5568366_5568367delinsGA , CM000669.1:g.5568366_5568367delinsGA GRCh37
NC_000007.12:g.5534892_5534893delinsGA NCBI36
NG_007992.1:g.6866_6867delinsTC , LRG_132:g.6866_6867delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-17_364-16delinsTC ENSP00000407473.2:n.364-17_364-16delinsTC
ENST00000473257.3:c.235-17_235-16delinsTC ENSP00000501773.1:n.235-17_235-16delinsTC
ENST00000477812.2:n.894_895delinsTC
ENST00000484841.6:n.559-17_559-16delinsTC
ENST00000493945.6:c.364-17_364-16delinsTC ENSP00000494269.1:n.364-17_364-16delinsTC
ENST00000642480.2:c.364-17_364-16delinsTC ENSP00000495995.2:n.364-17_364-16delinsTC
ENST00000645576.1:c.364-65_364-64delinsTC ENSP00000496101.1:n.364-65_364-64delinsTC
ENST00000646664.1:c.364-17_364-16delinsTC MANE Select ENSP00000494750.1:n.364-17_364-16delinsTC
ENST00000647275.1:c.-3-17_-3-16delinsTC ENSP00000494185.1:n.-3-17_-3-16delinsTC
ENST00000674681.1:c.364-17_364-16delinsTC ENSP00000502821.1:n.364-17_364-16delinsTC
ENST00000675515.1:c.364-17_364-16delinsTC ENSP00000501862.1:n.364-17_364-16delinsTC
ENST00000676189.1:c.375-29_375-28delinsTC ENSP00000502538.1:n.375-29_375-28delinsTC
ENST00000676319.1:c.87+835_87+836delinsTC ENSP00000502193.1:n.87+835_87+836delinsTC
ENST00000676397.1:c.364-17_364-16delinsTC ENSP00000502286.1:n.364-17_364-16delinsTC
ENST00000331789.9:c.364-17_364-16delinsTC ENSP00000349960.4:n.364-17_364-16delinsTC
ENST00000425660.5:c.*27-17_*27-16delinsTC ENSP00000409264.1:n.*27-17_*27-16delinsTC
ENST00000432588.5:c.364-17_364-16delinsTC ENSP00000407473.1:n.364-17_364-16delinsTC
ENST00000462494.5:n.872_873delinsTC
ENST00000473257.1:n.82-17_82-16delinsTC
ENST00000477812.1:n.571-17_571-16delinsTC
ENST00000484841.5:n.519-17_519-16delinsTC
ENST00000493945.5:n.370-17_370-16delinsTC
NM_001101.3:c.364-17_364-16delinsTC , LRG_132t1:c.364-17_364-16delinsTC NP_001092.1:n.364-17_364-16delinsTC
XM_006715764.1:c.-20_-19delinsTC XP_006715827.1:n.-20_-19delinsTC
NM_001101.4:c.364-17_364-16delinsTC NP_001092.1:n.364-17_364-16delinsTC
NM_001101.5:c.364-17_364-16delinsTC MANE Select NP_001092.1:n.364-17_364-16delinsTC