Canonical Allele Identifier: CA2681649658
Gene: ACTB HGNC NCBI

Linked Data

dbSNP Id: rs2128241311

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528725_5528726insTCTTCTCGCGGTTGGCCTTG , CM000669.2:g.5528725_5528726insTCTTCTCGCGGTTGGCCTTG GRCh38
NC_000007.13:g.5568356_5568357insTCTTCTCGCGGTTGGCCTTG , CM000669.1:g.5568356_5568357insTCTTCTCGCGGTTGGCCTTG GRCh37
NC_000007.12:g.5534882_5534883insTCTTCTCGCGGTTGGCCTTG NCBI36
NG_007992.1:g.6876_6877insCAAGGCCAACCGCGAGAAGA , LRG_132:g.6876_6877insCAAGGCCAACCGCGAGAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000407473.2:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000473257.3:c.235-7_235-6insCAAGGCCAACCGCGAGAAGA ENSP00000501773.1:n.235-7_235-6insCAAGGCCAACCGCGAGAAGA
ENST00000477812.2:n.904_905insCAAGGCCAACCGCGAGAAGA
ENST00000484841.6:n.559-7_559-6insCAAGGCCAACCGCGAGAAGA
ENST00000493945.6:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000494269.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000642480.2:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000495995.2:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000645576.1:c.364-55_364-54insCAAGGCCAACCGCGAGAAGA ENSP00000496101.1:n.364-55_364-54insCAAGGCCAACCGCGAGAAGA
ENST00000646664.1:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA MANE Select ENSP00000494750.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000647275.1:c.-3-7_-3-6insCAAGGCCAACCGCGAGAAGA ENSP00000494185.1:n.-3-7_-3-6insCAAGGCCAACCGCGAGAAGA
ENST00000674681.1:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000502821.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000675515.1:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000501862.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000676189.1:c.375-19_375-18insCAAGGCCAACCGCGAGAAGA ENSP00000502538.1:n.375-19_375-18insCAAGGCCAACCGCGAGAAGA
ENST00000676319.1:c.87+845_87+846insCAAGGCCAACCGCGAGAAGA ENSP00000502193.1:n.87+845_87+846insCAAGGCCAACCGCGAGAAGA
ENST00000676397.1:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000502286.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000331789.9:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000349960.4:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000425660.5:c.*27-7_*27-6insCAAGGCCAACCGCGAGAAGA ENSP00000409264.1:n.*27-7_*27-6insCAAGGCCAACCGCGAGAAGA
ENST00000432588.5:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA ENSP00000407473.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
ENST00000462494.5:n.882_883insCAAGGCCAACCGCGAGAAGA
ENST00000473257.1:n.82-7_82-6insCAAGGCCAACCGCGAGAAGA
ENST00000477812.1:n.571-7_571-6insCAAGGCCAACCGCGAGAAGA
ENST00000484841.5:n.519-7_519-6insCAAGGCCAACCGCGAGAAGA
ENST00000493945.5:n.370-7_370-6insCAAGGCCAACCGCGAGAAGA
NM_001101.3:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA , LRG_132t1:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA NP_001092.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
XM_006715764.1:c.-10_-9insCAAGGCCAACCGCGAGAAGA XP_006715827.1:n.-10_-9insCAAGGCCAACCGCGAGAAGA
NM_001101.4:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA NP_001092.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA
NM_001101.5:c.364-7_364-6insCAAGGCCAACCGCGAGAAGA MANE Select NP_001092.1:n.364-7_364-6insCAAGGCCAACCGCGAGAAGA