Canonical Allele Identifier: CA1684976255

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528884G= , CM000669.2:g.5528884G=	GRCh38
NC_000007.13:g.5568515G= , CM000669.1:g.5568515G=	GRCh37
NC_000007.12:g.5535041G=	NCBI36
NG_007992.1:g.6718C= , LRG_132:g.6718C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-165C=	ENSP00000407473.2:n.364-165C=
ENST00000473257.3:c.235-165C=	ENSP00000501773.1:n.235-165C=
ENST00000477812.2:n.746C=
ENST00000484841.6:n.558+135C=
ENST00000493945.6:c.364-165C=	ENSP00000494269.1:n.364-165C=
ENST00000642480.2:c.364-165C=	ENSP00000495995.2:n.364-165C=
ENST00000645576.1:c.364-213C=	ENSP00000496101.1:n.364-213C=
ENST00000646664.1:c.364-165C= MANE Select	ENSP00000494750.1:n.364-165C=
ENST00000647275.1:c.-3-165C=	ENSP00000494185.1:n.-3-165C=
ENST00000674681.1:c.364-165C=	ENSP00000502821.1:n.364-165C=
ENST00000675515.1:c.364-165C=	ENSP00000501862.1:n.364-165C=
ENST00000676189.1:c.375-177C=	ENSP00000502538.1:n.375-177C=
ENST00000676319.1:c.87+687C=	ENSP00000502193.1:n.87+687C=
ENST00000676397.1:c.364-165C=	ENSP00000502286.1:n.364-165C=
ENST00000331789.9:c.364-165C=	ENSP00000349960.4:n.364-165C=
ENST00000425660.5:c.*26+135C=	ENSP00000409264.1:n.*26+135C=
ENST00000432588.5:c.364-165C=	ENSP00000407473.1:n.364-165C=
ENST00000462494.5:n.724C=
ENST00000473257.1:n.82-165C=
ENST00000477812.1:n.571-165C=
ENST00000484841.5:n.519-165C=
ENST00000493945.5:n.370-165C=
NM_001101.3:c.364-165C= , LRG_132t1:c.364-165C=	NP_001092.1:n.364-165C=
XM_006715764.1:c.-168C=	XP_006715827.1:n.-168C=
NM_001101.4:c.364-165C=	NP_001092.1:n.364-165C=
NM_001101.5:c.364-165C= MANE Select	NP_001092.1:n.364-165C=