Canonical Allele Identifier: CA2681649749
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528846_5528857del , CM000669.2:g.5528846_5528857del GRCh38
NC_000007.13:g.5568477_5568488del , CM000669.1:g.5568477_5568488del GRCh37
NC_000007.12:g.5535003_5535014del NCBI36
NG_007992.1:g.6745_6756del , LRG_132:g.6745_6756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-138_364-127del ENSP00000407473.2:n.364-138_364-127del
ENST00000473257.3:c.235-138_235-127del ENSP00000501773.1:n.235-138_235-127del
ENST00000477812.2:n.773_784del
ENST00000484841.6:n.559-138_559-127del
ENST00000493945.6:c.364-138_364-127del ENSP00000494269.1:n.364-138_364-127del
ENST00000642480.2:c.364-138_364-127del ENSP00000495995.2:n.364-138_364-127del
ENST00000645576.1:c.364-186_364-175del ENSP00000496101.1:n.364-186_364-175del
ENST00000646664.1:c.364-138_364-127del MANE Select ENSP00000494750.1:n.364-138_364-127del
ENST00000647275.1:c.-3-138_-3-127del ENSP00000494185.1:n.-3-138_-3-127del
ENST00000674681.1:c.364-138_364-127del ENSP00000502821.1:n.364-138_364-127del
ENST00000675515.1:c.364-138_364-127del ENSP00000501862.1:n.364-138_364-127del
ENST00000676189.1:c.375-150_375-139del ENSP00000502538.1:n.375-150_375-139del
ENST00000676319.1:c.87+714_87+725del ENSP00000502193.1:n.87+714_87+725del
ENST00000676397.1:c.364-138_364-127del ENSP00000502286.1:n.364-138_364-127del
ENST00000331789.9:c.364-138_364-127del ENSP00000349960.4:n.364-138_364-127del
ENST00000425660.5:c.*27-138_*27-127del ENSP00000409264.1:n.*27-138_*27-127del
ENST00000432588.5:c.364-138_364-127del ENSP00000407473.1:n.364-138_364-127del
ENST00000462494.5:n.751_762del
ENST00000473257.1:n.82-138_82-127del
ENST00000477812.1:n.571-138_571-127del
ENST00000484841.5:n.519-138_519-127del
ENST00000493945.5:n.370-138_370-127del
NM_001101.3:c.364-138_364-127del , LRG_132t1:c.364-138_364-127del NP_001092.1:n.364-138_364-127del
XM_006715764.1:c.-141_-130del XP_006715827.1:n.-141_-130del
NM_001101.4:c.364-138_364-127del NP_001092.1:n.364-138_364-127del
NM_001101.5:c.364-138_364-127del MANE Select NP_001092.1:n.364-138_364-127del