Canonical Allele Identifier: CA2774259219

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528397del , CM000669.2:g.5528397del	GRCh38
NC_000007.13:g.5568028del , CM000669.1:g.5568028del	GRCh37
NC_000007.12:g.5534554del	NCBI36
NG_007992.1:g.7205del , LRG_132:g.7205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.686del	ENSP00000407473.2:p.Thr229ArgfsTer?
ENST00000473257.3:c.557del	ENSP00000501773.1:p.Thr186ArgfsTer?
ENST00000477812.2:n.1233del
ENST00000493945.6:c.686del	ENSP00000494269.1:p.Thr229ArgfsTer?
ENST00000642480.2:c.686del	ENSP00000495995.2:p.Thr229ArgfsTer?
ENST00000645576.1:c.638del	ENSP00000496101.1:p.Thr213ArgfsTer?
ENST00000646664.1:c.686del MANE Select	ENSP00000494750.1:p.Thr229ArgfsTer?
ENST00000647275.1:c.320del	ENSP00000494185.1:p.Thr107ArgfsTer?
ENST00000674681.1:c.686del	ENSP00000502821.1:p.Thr229ArgfsTer?
ENST00000675515.1:c.686del	ENSP00000501862.1:p.Thr229ArgfsTer?
ENST00000676189.1:c.*229del	ENSP00000502538.1:n.*229del
ENST00000676319.1:c.88-614del	ENSP00000502193.1:n.88-614del
ENST00000676397.1:c.686del	ENSP00000502286.1:p.Thr229ArgfsTer?
ENST00000331789.9:c.686del	ENSP00000349960.4:p.Thr229ArgfsTer?
ENST00000425660.5:c.*349del	ENSP00000409264.1:n.*349del
ENST00000462494.5:n.1211del
ENST00000473257.1:n.404del
ENST00000484841.5:n.841del
ENST00000493945.5:n.692del
NM_001101.3:c.686del , LRG_132t1:c.686del	NP_001092.1:p.Thr229ArgfsTer?
XM_006715764.1:c.320del	XP_006715827.1:p.Thr107ArgfsTer?
NM_001101.4:c.686del	NP_001092.1:p.Thr229ArgfsTer?
NM_001101.5:c.686del MANE Select	NP_001092.1:p.Thr229ArgfsTer?