Canonical Allele Identifier: CA2681649767
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528861_5528868del , CM000669.2:g.5528861_5528868del GRCh38
NC_000007.13:g.5568492_5568499del , CM000669.1:g.5568492_5568499del GRCh37
NC_000007.12:g.5535018_5535025del NCBI36
NG_007992.1:g.6734_6741del , LRG_132:g.6734_6741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-149_364-142del ENSP00000407473.2:n.364-149_364-142del
ENST00000473257.3:c.235-149_235-142del ENSP00000501773.1:n.235-149_235-142del
ENST00000477812.2:n.762_769del
ENST00000484841.6:n.559-149_559-142del
ENST00000493945.6:c.364-149_364-142del ENSP00000494269.1:n.364-149_364-142del
ENST00000642480.2:c.364-149_364-142del ENSP00000495995.2:n.364-149_364-142del
ENST00000645576.1:c.364-197_364-190del ENSP00000496101.1:n.364-197_364-190del
ENST00000646664.1:c.364-149_364-142del MANE Select ENSP00000494750.1:n.364-149_364-142del
ENST00000647275.1:c.-3-149_-3-142del ENSP00000494185.1:n.-3-149_-3-142del
ENST00000674681.1:c.364-149_364-142del ENSP00000502821.1:n.364-149_364-142del
ENST00000675515.1:c.364-149_364-142del ENSP00000501862.1:n.364-149_364-142del
ENST00000676189.1:c.375-161_375-154del ENSP00000502538.1:n.375-161_375-154del
ENST00000676319.1:c.87+703_87+710del ENSP00000502193.1:n.87+703_87+710del
ENST00000676397.1:c.364-149_364-142del ENSP00000502286.1:n.364-149_364-142del
ENST00000331789.9:c.364-149_364-142del ENSP00000349960.4:n.364-149_364-142del
ENST00000425660.5:c.*27-149_*27-142del ENSP00000409264.1:n.*27-149_*27-142del
ENST00000432588.5:c.364-149_364-142del ENSP00000407473.1:n.364-149_364-142del
ENST00000462494.5:n.740_747del
ENST00000473257.1:n.82-149_82-142del
ENST00000477812.1:n.571-149_571-142del
ENST00000484841.5:n.519-149_519-142del
ENST00000493945.5:n.370-149_370-142del
NM_001101.3:c.364-149_364-142del , LRG_132t1:c.364-149_364-142del NP_001092.1:n.364-149_364-142del
XM_006715764.1:c.-152_-145del XP_006715827.1:n.-152_-145del
NM_001101.4:c.364-149_364-142del NP_001092.1:n.364-149_364-142del
NM_001101.5:c.364-149_364-142del MANE Select NP_001092.1:n.364-149_364-142del