Canonical Allele Identifier: CA1684976534

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529022_5529024delinsCAG , CM000669.2:g.5529022_5529024delinsCAG	GRCh38
NC_000007.13:g.5568653_5568655delinsCAG , CM000669.1:g.5568653_5568655delinsCAG	GRCh37
NC_000007.12:g.5535179_5535181delinsCAG	NCBI36
NG_007992.1:g.6578_6580delinsCTG , LRG_132:g.6578_6580delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+137_363+139delinsCTG	ENSP00000407473.2:n.363+137_363+139delinsCTG
ENST00000473257.3:c.234+137_234+139delinsCTG	ENSP00000501773.1:n.234+137_234+139delinsCTG
ENST00000477812.2:n.606_608delinsCTG
ENST00000484841.6:n.553_555delinsCTG
ENST00000493945.6:c.363+137_363+139delinsCTG	ENSP00000494269.1:n.363+137_363+139delinsCTG
ENST00000642480.2:c.363+137_363+139delinsCTG	ENSP00000495995.2:n.363+137_363+139delinsCTG
ENST00000645025.1:n.482_484delinsCTG
ENST00000645576.1:c.363+137_363+139delinsCTG	ENSP00000496101.1:n.363+137_363+139delinsCTG
ENST00000646664.1:c.363+137_363+139delinsCTG MANE Select	ENSP00000494750.1:n.363+137_363+139delinsCTG
ENST00000647275.1:c.-3-305_-3-303delinsCTG	ENSP00000494185.1:n.-3-305_-3-303delinsCTG
ENST00000674681.1:c.363+137_363+139delinsCTG	ENSP00000502821.1:n.363+137_363+139delinsCTG
ENST00000675515.1:c.363+137_363+139delinsCTG	ENSP00000501862.1:n.363+137_363+139delinsCTG
ENST00000676189.1:c.374+126_374+128delinsCTG	ENSP00000502538.1:n.374+126_374+128delinsCTG
ENST00000676319.1:c.87+547_87+549delinsCTG	ENSP00000502193.1:n.87+547_87+549delinsCTG
ENST00000676397.1:c.363+137_363+139delinsCTG	ENSP00000502286.1:n.363+137_363+139delinsCTG
ENST00000331789.9:c.363+137_363+139delinsCTG	ENSP00000349960.4:n.363+137_363+139delinsCTG
ENST00000425660.5:c.*21_*23delinsCTG	ENSP00000409264.1:n.*21_*23delinsCTG
ENST00000432588.5:c.363+137_363+139delinsCTG	ENSP00000407473.1:n.363+137_363+139delinsCTG
ENST00000462494.5:n.584_586delinsCTG
ENST00000473257.1:n.82-305_82-303delinsCTG
ENST00000477812.1:n.570+137_570+139delinsCTG
ENST00000484841.5:n.518+137_518+139delinsCTG
ENST00000493945.5:n.369+137_369+139delinsCTG
NM_001101.3:c.363+137_363+139delinsCTG , LRG_132t1:c.363+137_363+139delinsCTG	NP_001092.1:n.363+137_363+139delinsCTG
XM_006715764.1:c.-308_-306delinsCTG	XP_006715827.1:n.-308_-306delinsCTG
NM_001101.4:c.363+137_363+139delinsCTG	NP_001092.1:n.363+137_363+139delinsCTG
NM_001101.5:c.363+137_363+139delinsCTG MANE Select	NP_001092.1:n.363+137_363+139delinsCTG