Canonical Allele Identifier: CA1684976871

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529177C= , CM000669.2:g.5529177C=	GRCh38
NC_000007.13:g.5568808C= , CM000669.1:g.5568808C=	GRCh37
NC_000007.12:g.5535334C=	NCBI36
NG_007992.1:g.6425G= , LRG_132:g.6425G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.347G=	ENSP00000407473.2:p.Arg116=
ENST00000473257.3:c.218G=	ENSP00000501773.1:p.Arg73=
ENST00000477812.2:n.554G=
ENST00000484841.6:n.501G=
ENST00000493945.6:c.347G=	ENSP00000494269.1:p.Arg116=
ENST00000642480.2:c.347G=	ENSP00000495995.2:p.Arg116=
ENST00000645025.1:n.430G=
ENST00000645576.1:c.347G=	ENSP00000496101.1:p.Arg116=
ENST00000646664.1:c.347G= MANE Select	ENSP00000494750.1:p.Arg116=
ENST00000647275.1:c.-3-458G=	ENSP00000494185.1:n.-3-458G=
ENST00000674681.1:c.347G=	ENSP00000502821.1:p.Arg116=
ENST00000675515.1:c.347G=	ENSP00000501862.1:p.Arg116=
ENST00000676189.1:c.347G=	ENSP00000502538.1:p.Arg116=
ENST00000676319.1:c.87+394G=	ENSP00000502193.1:n.87+394G=
ENST00000676397.1:c.347G=	ENSP00000502286.1:p.Arg116=
ENST00000331789.9:c.347G=	ENSP00000349960.4:p.Arg116=
ENST00000425660.5:c.347G=	ENSP00000409264.1:p.Arg116=
ENST00000432588.5:c.347G=	ENSP00000407473.1:p.Arg116=
ENST00000462494.5:n.431G=
ENST00000473257.1:n.82-458G=
ENST00000477812.1:n.554G=
ENST00000480301.1:n.547G=
ENST00000484841.5:n.502G=
ENST00000493945.5:n.353G=
NM_001101.3:c.347G= , LRG_132t1:c.347G=	NP_001092.1:p.Arg116=
XM_006715764.1:c.-360G=	XP_006715827.1:n.-360G=
NM_001101.4:c.347G=	NP_001092.1:p.Arg116=
NM_001101.5:c.347G= MANE Select	NP_001092.1:p.Arg116=