Canonical Allele Identifier: CA1684987992

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528405C= , CM000669.2:g.5528405C=	GRCh38
NC_000007.13:g.5568036C= , CM000669.1:g.5568036C=	GRCh37
NC_000007.12:g.5534562C=	NCBI36
NG_007992.1:g.7197G= , LRG_132:g.7197G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.678G=	ENSP00000407473.2:p.Glu226=
ENST00000473257.3:c.549G=	ENSP00000501773.1:p.Glu183=
ENST00000477812.2:n.1225G=
ENST00000493945.6:c.678G=	ENSP00000494269.1:p.Glu226=
ENST00000642480.2:c.678G=	ENSP00000495995.2:p.Glu226=
ENST00000645576.1:c.630G=	ENSP00000496101.1:p.Glu210=
ENST00000646664.1:c.678G= MANE Select	ENSP00000494750.1:p.Glu226=
ENST00000647275.1:c.312G=	ENSP00000494185.1:p.Glu104=
ENST00000674681.1:c.678G=	ENSP00000502821.1:p.Glu226=
ENST00000675515.1:c.678G=	ENSP00000501862.1:p.Glu226=
ENST00000676189.1:c.*221G=	ENSP00000502538.1:n.*221G=
ENST00000676319.1:c.88-622G=	ENSP00000502193.1:n.88-622G=
ENST00000676397.1:c.678G=	ENSP00000502286.1:p.Glu226=
ENST00000331789.9:c.678G=	ENSP00000349960.4:p.Glu226=
ENST00000425660.5:c.*341G=	ENSP00000409264.1:n.*341G=
ENST00000462494.5:n.1203G=
ENST00000473257.1:n.396G=
ENST00000484841.5:n.833G=
ENST00000493945.5:n.684G=
NM_001101.3:c.678G= , LRG_132t1:c.678G=	NP_001092.1:p.Glu226=
XM_006715764.1:c.312G=	XP_006715827.1:p.Glu104=
NM_001101.4:c.678G=	NP_001092.1:p.Glu226=
NM_001101.5:c.678G= MANE Select	NP_001092.1:p.Glu226=