Canonical Allele Identifier: CA1684975891

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528654G= , CM000669.2:g.5528654G=	GRCh38
NC_000007.13:g.5568285G= , CM000669.1:g.5568285G=	GRCh37
NC_000007.12:g.5534811G=	NCBI36
NG_007992.1:g.6948C= , LRG_132:g.6948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.429C=	ENSP00000407473.2:p.Tyr143=
ENST00000473257.3:c.300C=	ENSP00000501773.1:p.Tyr100=
ENST00000477812.2:n.976C=
ENST00000493945.6:c.429C=	ENSP00000494269.1:p.Tyr143=
ENST00000642480.2:c.429C=	ENSP00000495995.2:p.Tyr143=
ENST00000645576.1:c.381C=	ENSP00000496101.1:p.Tyr127=
ENST00000646664.1:c.429C= MANE Select	ENSP00000494750.1:p.Tyr143=
ENST00000647275.1:c.63C=	ENSP00000494185.1:p.Tyr21=
ENST00000674681.1:c.429C=	ENSP00000502821.1:p.Tyr143=
ENST00000675515.1:c.429C=	ENSP00000501862.1:p.Tyr143=
ENST00000676189.1:c.428C=	ENSP00000502538.1:p.Thr143=
ENST00000676319.1:c.88-871C=	ENSP00000502193.1:n.88-871C=
ENST00000676397.1:c.429C=	ENSP00000502286.1:p.Tyr143=
ENST00000331789.9:c.429C=	ENSP00000349960.4:p.Tyr143=
ENST00000425660.5:c.*92C=	ENSP00000409264.1:n.*92C=
ENST00000432588.5:c.429C=	ENSP00000407473.1:p.Tyr143=
ENST00000462494.5:n.954C=
ENST00000473257.1:n.147C=
ENST00000477812.1:n.636C=
ENST00000484841.5:n.584C=
ENST00000493945.5:n.435C=
NM_001101.3:c.429C= , LRG_132t1:c.429C=	NP_001092.1:p.Tyr143=
XM_006715764.1:c.63C=	XP_006715827.1:p.Tyr21=
NM_001101.4:c.429C=	NP_001092.1:p.Tyr143=
NM_001101.5:c.429C= MANE Select	NP_001092.1:p.Tyr143=