Canonical Allele Identifier: CA2681649859

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528954-T-TCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528954_5528955insCTC , CM000669.2:g.5528954_5528955insCTC	GRCh38
NC_000007.13:g.5568585_5568586insCTC , CM000669.1:g.5568585_5568586insCTC	GRCh37
NC_000007.12:g.5535111_5535112insCTC	NCBI36
NG_007992.1:g.6647_6648insGAG , LRG_132:g.6647_6648insGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+206_363+207insGAG	ENSP00000407473.2:n.363+206_363+207insGAG
ENST00000473257.3:c.234+206_234+207insGAG	ENSP00000501773.1:n.234+206_234+207insGAG
ENST00000477812.2:n.675_676insGAG
ENST00000484841.6:n.558+64_558+65insGAG
ENST00000493945.6:c.363+206_363+207insGAG	ENSP00000494269.1:n.363+206_363+207insGAG
ENST00000642480.2:c.363+206_363+207insGAG	ENSP00000495995.2:n.363+206_363+207insGAG
ENST00000645025.1:n.551_552insGAG
ENST00000645576.1:c.363+206_363+207insGAG	ENSP00000496101.1:n.363+206_363+207insGAG
ENST00000646664.1:c.363+206_363+207insGAG MANE Select	ENSP00000494750.1:n.363+206_363+207insGAG
ENST00000647275.1:c.-3-236_-3-235insGAG	ENSP00000494185.1:n.-3-236_-3-235insGAG
ENST00000674681.1:c.363+206_363+207insGAG	ENSP00000502821.1:n.363+206_363+207insGAG
ENST00000675515.1:c.363+206_363+207insGAG	ENSP00000501862.1:n.363+206_363+207insGAG
ENST00000676189.1:c.374+195_374+196insGAG	ENSP00000502538.1:n.374+195_374+196insGAG
ENST00000676319.1:c.87+616_87+617insGAG	ENSP00000502193.1:n.87+616_87+617insGAG
ENST00000676397.1:c.363+206_363+207insGAG	ENSP00000502286.1:n.363+206_363+207insGAG
ENST00000331789.9:c.363+206_363+207insGAG	ENSP00000349960.4:n.363+206_363+207insGAG
ENST00000425660.5:c.*26+64_*26+65insGAG	ENSP00000409264.1:n.*26+64_*26+65insGAG
ENST00000432588.5:c.363+206_363+207insGAG	ENSP00000407473.1:n.363+206_363+207insGAG
ENST00000462494.5:n.653_654insGAG
ENST00000473257.1:n.82-236_82-235insGAG
ENST00000477812.1:n.570+206_570+207insGAG
ENST00000484841.5:n.518+206_518+207insGAG
ENST00000493945.5:n.369+206_369+207insGAG
NM_001101.3:c.363+206_363+207insGAG , LRG_132t1:c.363+206_363+207insGAG	NP_001092.1:n.363+206_363+207insGAG
XM_006715764.1:c.-239_-238insGAG	XP_006715827.1:n.-239_-238insGAG
NM_001101.4:c.363+206_363+207insGAG	NP_001092.1:n.363+206_363+207insGAG
NM_001101.5:c.363+206_363+207insGAG MANE Select	NP_001092.1:n.363+206_363+207insGAG