Canonical Allele Identifier: CA1684975851

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528615A= , CM000669.2:g.5528615A=	GRCh38
NC_000007.13:g.5568246A= , CM000669.1:g.5568246A=	GRCh37
NC_000007.12:g.5534772A=	NCBI36
NG_007992.1:g.6987T= , LRG_132:g.6987T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.468T=	ENSP00000407473.2:p.Gly156=
ENST00000473257.3:c.339T=	ENSP00000501773.1:p.Gly113=
ENST00000477812.2:n.1015T=
ENST00000493945.6:c.468T=	ENSP00000494269.1:p.Gly156=
ENST00000642480.2:c.468T=	ENSP00000495995.2:p.Gly156=
ENST00000645576.1:c.420T=	ENSP00000496101.1:p.Gly140=
ENST00000646664.1:c.468T= MANE Select	ENSP00000494750.1:p.Gly156=
ENST00000647275.1:c.102T=	ENSP00000494185.1:p.Gly34=
ENST00000674681.1:c.468T=	ENSP00000502821.1:p.Gly156=
ENST00000675515.1:c.468T=	ENSP00000501862.1:p.Gly156=
ENST00000676189.1:c.*11T=	ENSP00000502538.1:n.*11T=
ENST00000676319.1:c.88-832T=	ENSP00000502193.1:n.88-832T=
ENST00000676397.1:c.468T=	ENSP00000502286.1:p.Gly156=
ENST00000331789.9:c.468T=	ENSP00000349960.4:p.Gly156=
ENST00000425660.5:c.*131T=	ENSP00000409264.1:n.*131T=
ENST00000432588.5:c.468T=	ENSP00000407473.1:p.Gly156=
ENST00000462494.5:n.993T=
ENST00000473257.1:n.186T=
ENST00000477812.1:n.675T=
ENST00000484841.5:n.623T=
ENST00000493945.5:n.474T=
NM_001101.3:c.468T= , LRG_132t1:c.468T=	NP_001092.1:p.Gly156=
XM_006715764.1:c.102T=	XP_006715827.1:p.Gly34=
NM_001101.4:c.468T=	NP_001092.1:p.Gly156=
NM_001101.5:c.468T= MANE Select	NP_001092.1:p.Gly156=