Canonical Allele Identifier: CA2681649925
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529076_5529079del , CM000669.2:g.5529076_5529079del GRCh38
NC_000007.13:g.5568707_5568710del , CM000669.1:g.5568707_5568710del GRCh37
NC_000007.12:g.5535233_5535236del NCBI36
NG_007992.1:g.6523_6526del , LRG_132:g.6523_6526del

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.363+82_363+85del ENSP00000407473.2:n.363+82_363+85del
ENST00000473257.3:c.234+82_234+85del ENSP00000501773.1:n.234+82_234+85del
ENST00000477812.2:n.571-20_571-17del
ENST00000484841.6:n.518-20_518-17del
ENST00000493945.6:c.363+82_363+85del ENSP00000494269.1:n.363+82_363+85del
ENST00000642480.2:c.363+82_363+85del ENSP00000495995.2:n.363+82_363+85del
ENST00000645025.1:n.447-20_447-17del
ENST00000645576.1:c.363+82_363+85del ENSP00000496101.1:n.363+82_363+85del
ENST00000646664.1:c.363+82_363+85del MANE Select ENSP00000494750.1:n.363+82_363+85del
ENST00000647275.1:c.-3-360_-3-357del ENSP00000494185.1:n.-3-360_-3-357del
ENST00000674681.1:c.363+82_363+85del ENSP00000502821.1:n.363+82_363+85del
ENST00000675515.1:c.363+82_363+85del ENSP00000501862.1:n.363+82_363+85del
ENST00000676189.1:c.374+71_374+74del ENSP00000502538.1:n.374+71_374+74del
ENST00000676319.1:c.87+492_87+495del ENSP00000502193.1:n.87+492_87+495del
ENST00000676397.1:c.363+82_363+85del ENSP00000502286.1:n.363+82_363+85del
ENST00000331789.9:c.363+82_363+85del ENSP00000349960.4:n.363+82_363+85del
ENST00000425660.5:c.364-20_364-17del ENSP00000409264.1:n.364-20_364-17del
ENST00000432588.5:c.363+82_363+85del ENSP00000407473.1:n.363+82_363+85del
ENST00000462494.5:n.529_532del
ENST00000473257.1:n.82-360_82-357del
ENST00000477812.1:n.570+82_570+85del
ENST00000480301.1:n.645_648del
ENST00000484841.5:n.518+82_518+85del
ENST00000493945.5:n.369+82_369+85del
NM_001101.3:c.363+82_363+85del , LRG_132t1:c.363+82_363+85del NP_001092.1:n.363+82_363+85del
XM_006715764.1:c.-343-20_-343-17del XP_006715827.1:n.-343-20_-343-17del
NM_001101.4:c.363+82_363+85del NP_001092.1:n.363+82_363+85del
NM_001101.5:c.363+82_363+85del MANE Select NP_001092.1:n.363+82_363+85del