Canonical Allele Identifier: CA1684976672

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529082G= , CM000669.2:g.5529082G=	GRCh38
NC_000007.13:g.5568713G= , CM000669.1:g.5568713G=	GRCh37
NC_000007.12:g.5535239G=	NCBI36
NG_007992.1:g.6520C= , LRG_132:g.6520C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+79C=	ENSP00000407473.2:n.363+79C=
ENST00000473257.3:c.234+79C=	ENSP00000501773.1:n.234+79C=
ENST00000477812.2:n.571-23C=
ENST00000484841.6:n.518-23C=
ENST00000493945.6:c.363+79C=	ENSP00000494269.1:n.363+79C=
ENST00000642480.2:c.363+79C=	ENSP00000495995.2:n.363+79C=
ENST00000645025.1:n.447-23C=
ENST00000645576.1:c.363+79C=	ENSP00000496101.1:n.363+79C=
ENST00000646664.1:c.363+79C= MANE Select	ENSP00000494750.1:n.363+79C=
ENST00000647275.1:c.-3-363C=	ENSP00000494185.1:n.-3-363C=
ENST00000674681.1:c.363+79C=	ENSP00000502821.1:n.363+79C=
ENST00000675515.1:c.363+79C=	ENSP00000501862.1:n.363+79C=
ENST00000676189.1:c.374+68C=	ENSP00000502538.1:n.374+68C=
ENST00000676319.1:c.87+489C=	ENSP00000502193.1:n.87+489C=
ENST00000676397.1:c.363+79C=	ENSP00000502286.1:n.363+79C=
ENST00000331789.9:c.363+79C=	ENSP00000349960.4:n.363+79C=
ENST00000425660.5:c.364-23C=	ENSP00000409264.1:n.364-23C=
ENST00000432588.5:c.363+79C=	ENSP00000407473.1:n.363+79C=
ENST00000462494.5:n.526C=
ENST00000473257.1:n.82-363C=
ENST00000477812.1:n.570+79C=
ENST00000480301.1:n.642C=
ENST00000484841.5:n.518+79C=
ENST00000493945.5:n.369+79C=
NM_001101.3:c.363+79C= , LRG_132t1:c.363+79C=	NP_001092.1:n.363+79C=
XM_006715764.1:c.-343-23C=	XP_006715827.1:n.-343-23C=
NM_001101.4:c.363+79C=	NP_001092.1:n.363+79C=
NM_001101.5:c.363+79C= MANE Select	NP_001092.1:n.363+79C=