Canonical Allele Identifier: CA1684976567

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529042_5529043delinsAG , CM000669.2:g.5529042_5529043delinsAG	GRCh38
NC_000007.13:g.5568673_5568674delinsAG , CM000669.1:g.5568673_5568674delinsAG	GRCh37
NC_000007.12:g.5535199_5535200delinsAG	NCBI36
NG_007992.1:g.6559_6560delinsCT , LRG_132:g.6559_6560delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+118_363+119delinsCT	ENSP00000407473.2:n.363+118_363+119delinsCT
ENST00000473257.3:c.234+118_234+119delinsCT	ENSP00000501773.1:n.234+118_234+119delinsCT
ENST00000477812.2:n.587_588delinsCT
ENST00000484841.6:n.534_535delinsCT
ENST00000493945.6:c.363+118_363+119delinsCT	ENSP00000494269.1:n.363+118_363+119delinsCT
ENST00000642480.2:c.363+118_363+119delinsCT	ENSP00000495995.2:n.363+118_363+119delinsCT
ENST00000645025.1:n.463_464delinsCT
ENST00000645576.1:c.363+118_363+119delinsCT	ENSP00000496101.1:n.363+118_363+119delinsCT
ENST00000646664.1:c.363+118_363+119delinsCT MANE Select	ENSP00000494750.1:n.363+118_363+119delinsCT
ENST00000647275.1:c.-3-324_-3-323delinsCT	ENSP00000494185.1:n.-3-324_-3-323delinsCT
ENST00000674681.1:c.363+118_363+119delinsCT	ENSP00000502821.1:n.363+118_363+119delinsCT
ENST00000675515.1:c.363+118_363+119delinsCT	ENSP00000501862.1:n.363+118_363+119delinsCT
ENST00000676189.1:c.374+107_374+108delinsCT	ENSP00000502538.1:n.374+107_374+108delinsCT
ENST00000676319.1:c.87+528_87+529delinsCT	ENSP00000502193.1:n.87+528_87+529delinsCT
ENST00000676397.1:c.363+118_363+119delinsCT	ENSP00000502286.1:n.363+118_363+119delinsCT
ENST00000331789.9:c.363+118_363+119delinsCT	ENSP00000349960.4:n.363+118_363+119delinsCT
ENST00000425660.5:c.*2_*3delinsCT	ENSP00000409264.1:n.*2_*3delinsCT
ENST00000432588.5:c.363+118_363+119delinsCT	ENSP00000407473.1:n.363+118_363+119delinsCT
ENST00000462494.5:n.565_566delinsCT
ENST00000473257.1:n.82-324_82-323delinsCT
ENST00000477812.1:n.570+118_570+119delinsCT
ENST00000484841.5:n.518+118_518+119delinsCT
ENST00000493945.5:n.369+118_369+119delinsCT
NM_001101.3:c.363+118_363+119delinsCT , LRG_132t1:c.363+118_363+119delinsCT	NP_001092.1:n.363+118_363+119delinsCT
XM_006715764.1:c.-327_-326delinsCT	XP_006715827.1:n.-327_-326delinsCT
NM_001101.4:c.363+118_363+119delinsCT	NP_001092.1:n.363+118_363+119delinsCT
NM_001101.5:c.363+118_363+119delinsCT MANE Select	NP_001092.1:n.363+118_363+119delinsCT