Canonical Allele Identifier: CA2681649803
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528889_5528898del , CM000669.2:g.5528889_5528898del GRCh38
NC_000007.13:g.5568520_5568529del , CM000669.1:g.5568520_5568529del GRCh37
NC_000007.12:g.5535046_5535055del NCBI36
NG_007992.1:g.6704_6713del , LRG_132:g.6704_6713del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-179_364-170del ENSP00000407473.2:n.364-179_364-170del
ENST00000473257.3:c.235-179_235-170del ENSP00000501773.1:n.235-179_235-170del
ENST00000477812.2:n.732_741del
ENST00000484841.6:n.558+121_558+130del
ENST00000493945.6:c.364-179_364-170del ENSP00000494269.1:n.364-179_364-170del
ENST00000642480.2:c.364-179_364-170del ENSP00000495995.2:n.364-179_364-170del
ENST00000645576.1:c.364-227_364-218del ENSP00000496101.1:n.364-227_364-218del
ENST00000646664.1:c.364-179_364-170del MANE Select ENSP00000494750.1:n.364-179_364-170del
ENST00000647275.1:c.-3-179_-3-170del ENSP00000494185.1:n.-3-179_-3-170del
ENST00000674681.1:c.364-179_364-170del ENSP00000502821.1:n.364-179_364-170del
ENST00000675515.1:c.364-179_364-170del ENSP00000501862.1:n.364-179_364-170del
ENST00000676189.1:c.375-191_375-182del ENSP00000502538.1:n.375-191_375-182del
ENST00000676319.1:c.87+673_87+682del ENSP00000502193.1:n.87+673_87+682del
ENST00000676397.1:c.364-179_364-170del ENSP00000502286.1:n.364-179_364-170del
ENST00000331789.9:c.364-179_364-170del ENSP00000349960.4:n.364-179_364-170del
ENST00000425660.5:c.*26+121_*26+130del ENSP00000409264.1:n.*26+121_*26+130del
ENST00000432588.5:c.364-179_364-170del ENSP00000407473.1:n.364-179_364-170del
ENST00000462494.5:n.710_719del
ENST00000473257.1:n.82-179_82-170del
ENST00000477812.1:n.571-179_571-170del
ENST00000484841.5:n.519-179_519-170del
ENST00000493945.5:n.370-179_370-170del
NM_001101.3:c.364-179_364-170del , LRG_132t1:c.364-179_364-170del NP_001092.1:n.364-179_364-170del
XM_006715764.1:c.-182_-173del XP_006715827.1:n.-182_-173del
NM_001101.4:c.364-179_364-170del NP_001092.1:n.364-179_364-170del
NM_001101.5:c.364-179_364-170del MANE Select NP_001092.1:n.364-179_364-170del