Canonical Allele Identifier: CA2840896156

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528706dup , CM000669.2:g.5528706dup	GRCh38
NC_000007.13:g.5568337dup , CM000669.1:g.5568337dup	GRCh37
NC_000007.12:g.5534863dup	NCBI36
NG_007992.1:g.6897dup , LRG_132:g.6897dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.378dup	ENSP00000407473.2:p.Phe127LeufsTer?
ENST00000473257.3:c.249dup	ENSP00000501773.1:p.Phe84LeufsTer?
ENST00000477812.2:n.925dup
ENST00000493945.6:c.378dup	ENSP00000494269.1:p.Phe127LeufsTer?
ENST00000642480.2:c.378dup	ENSP00000495995.2:p.Phe127LeufsTer?
ENST00000645576.1:c.364-34dup	ENSP00000496101.1:n.364-34dup
ENST00000646664.1:c.378dup MANE Select	ENSP00000494750.1:p.Phe127LeufsTer?
ENST00000647275.1:c.12dup	ENSP00000494185.1:p.Phe5LeufsTer?
ENST00000674681.1:c.378dup	ENSP00000502821.1:p.Phe127LeufsTer?
ENST00000675515.1:c.378dup	ENSP00000501862.1:p.Phe127LeufsTer?
ENST00000676189.1:c.377dup	ENSP00000502538.1:p.Ser127PhefsTer?
ENST00000676319.1:c.87+866dup	ENSP00000502193.1:n.87+866dup
ENST00000676397.1:c.378dup	ENSP00000502286.1:p.Phe127LeufsTer?
ENST00000331789.9:c.378dup	ENSP00000349960.4:p.Phe127LeufsTer?
ENST00000425660.5:c.*41dup	ENSP00000409264.1:n.*41dup
ENST00000432588.5:c.378dup	ENSP00000407473.1:p.Phe127LeufsTer?
ENST00000462494.5:n.903dup
ENST00000473257.1:n.96dup
ENST00000477812.1:n.585dup
ENST00000484841.5:n.533dup
ENST00000493945.5:n.384dup
NM_001101.3:c.378dup , LRG_132t1:c.378dup	NP_001092.1:p.Phe127LeufsTer?
XM_006715764.1:c.12dup	XP_006715827.1:p.Phe5LeufsTer?
NM_001101.4:c.378dup	NP_001092.1:p.Phe127LeufsTer?
NM_001101.5:c.378dup MANE Select	NP_001092.1:p.Phe127LeufsTer?