Canonical Allele Identifier: CA2578822294

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529077_5529079del , CM000669.2:g.5529077_5529079del	GRCh38
NC_000007.13:g.5568708_5568710del , CM000669.1:g.5568708_5568710del	GRCh37
NC_000007.12:g.5535234_5535236del	NCBI36
NG_007992.1:g.6526_6528del , LRG_132:g.6526_6528del

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.363+85_363+87del	ENSP00000407473.2:n.363+85_363+87del
ENST00000473257.3:c.234+85_234+87del	ENSP00000501773.1:n.234+85_234+87del
ENST00000477812.2:n.571-17_571-15del
ENST00000484841.6:n.518-17_518-15del
ENST00000493945.6:c.363+85_363+87del	ENSP00000494269.1:n.363+85_363+87del
ENST00000642480.2:c.363+85_363+87del	ENSP00000495995.2:n.363+85_363+87del
ENST00000645025.1:n.447-17_447-15del
ENST00000645576.1:c.363+85_363+87del	ENSP00000496101.1:n.363+85_363+87del
ENST00000646664.1:c.363+85_363+87del MANE Select	ENSP00000494750.1:n.363+85_363+87del
ENST00000647275.1:c.-3-357_-3-355del	ENSP00000494185.1:n.-3-357_-3-355del
ENST00000674681.1:c.363+85_363+87del	ENSP00000502821.1:n.363+85_363+87del
ENST00000675515.1:c.363+85_363+87del	ENSP00000501862.1:n.363+85_363+87del
ENST00000676189.1:c.374+74_374+76del	ENSP00000502538.1:n.374+74_374+76del
ENST00000676319.1:c.87+495_87+497del	ENSP00000502193.1:n.87+495_87+497del
ENST00000676397.1:c.363+85_363+87del	ENSP00000502286.1:n.363+85_363+87del
ENST00000331789.9:c.363+85_363+87del	ENSP00000349960.4:n.363+85_363+87del
ENST00000425660.5:c.364-17_364-15del	ENSP00000409264.1:n.364-17_364-15del
ENST00000432588.5:c.363+85_363+87del	ENSP00000407473.1:n.363+85_363+87del
ENST00000462494.5:n.532_534del
ENST00000473257.1:n.82-357_82-355del
ENST00000477812.1:n.570+85_570+87del
ENST00000480301.1:n.648_650del
ENST00000484841.5:n.518+85_518+87del
ENST00000493945.5:n.369+85_369+87del
NM_001101.3:c.363+85_363+87del , LRG_132t1:c.363+85_363+87del	NP_001092.1:n.363+85_363+87del
XM_006715764.1:c.-343-17_-343-15del	XP_006715827.1:n.-343-17_-343-15del
NM_001101.4:c.363+85_363+87del	NP_001092.1:n.363+85_363+87del
NM_001101.5:c.363+85_363+87del MANE Select	NP_001092.1:n.363+85_363+87del