Canonical Allele Identifier: CA1097928539
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528722_5528723insGGTCATCTTCTCGCGGT , CM000669.2:g.5528722_5528723insGGTCATCTTCTCGCGGT GRCh38
NC_000007.13:g.5568353_5568354insGGTCATCTTCTCGCGGT , CM000669.1:g.5568353_5568354insGGTCATCTTCTCGCGGT GRCh37
NC_000007.12:g.5534879_5534880insGGTCATCTTCTCGCGGT NCBI36
NG_007992.1:g.6879_6880insACCGCGAGAAGATGACC , LRG_132:g.6879_6880insACCGCGAGAAGATGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000407473.2:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000473257.3:c.235-4_235-3insACCGCGAGAAGATGACC ENSP00000501773.1:n.235-4_235-3insACCGCGAGAAGATGACC
ENST00000477812.2:n.907_908insACCGCGAGAAGATGACC
ENST00000484841.6:n.559-4_559-3insACCGCGAGAAGATGACC
ENST00000493945.6:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000494269.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000642480.2:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000495995.2:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000645576.1:c.364-52_364-51insACCGCGAGAAGATGACC ENSP00000496101.1:n.364-52_364-51insACCGCGAGAAGATGACC
ENST00000646664.1:c.364-4_364-3insACCGCGAGAAGATGACC MANE Select ENSP00000494750.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000647275.1:c.-3-4_-3-3insACCGCGAGAAGATGACC ENSP00000494185.1:n.-3-4_-3-3insACCGCGAGAAGATGACC
ENST00000674681.1:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000502821.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000675515.1:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000501862.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000676189.1:c.375-16_375-15insACCGCGAGAAGATGACC ENSP00000502538.1:n.375-16_375-15insACCGCGAGAAGATGACC
ENST00000676319.1:c.87+848_87+849insACCGCGAGAAGATGACC ENSP00000502193.1:n.87+848_87+849insACCGCGAGAAGATGACC
ENST00000676397.1:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000502286.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000331789.9:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000349960.4:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000425660.5:c.*27-4_*27-3insACCGCGAGAAGATGACC ENSP00000409264.1:n.*27-4_*27-3insACCGCGAGAAGATGACC
ENST00000432588.5:c.364-4_364-3insACCGCGAGAAGATGACC ENSP00000407473.1:n.364-4_364-3insACCGCGAGAAGATGACC
ENST00000462494.5:n.885_886insACCGCGAGAAGATGACC
ENST00000473257.1:n.82-4_82-3insACCGCGAGAAGATGACC
ENST00000477812.1:n.571-4_571-3insACCGCGAGAAGATGACC
ENST00000484841.5:n.519-4_519-3insACCGCGAGAAGATGACC
ENST00000493945.5:n.370-4_370-3insACCGCGAGAAGATGACC
NM_001101.3:c.364-4_364-3insACCGCGAGAAGATGACC , LRG_132t1:c.364-4_364-3insACCGCGAGAAGATGACC NP_001092.1:n.364-4_364-3insACCGCGAGAAGATGACC
XM_006715764.1:c.-7_-6insACCGCGAGAAGATGACC XP_006715827.1:n.-7_-6insACCGCGAGAAGATGACC
NM_001101.4:c.364-4_364-3insACCGCGAGAAGATGACC NP_001092.1:n.364-4_364-3insACCGCGAGAAGATGACC
NM_001101.5:c.364-4_364-3insACCGCGAGAAGATGACC MANE Select NP_001092.1:n.364-4_364-3insACCGCGAGAAGATGACC