Canonical Allele Identifier: CA1684976682

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529088G= , CM000669.2:g.5529088G=	GRCh38
NC_000007.13:g.5568719G= , CM000669.1:g.5568719G=	GRCh37
NC_000007.12:g.5535245G=	NCBI36
NG_007992.1:g.6514C= , LRG_132:g.6514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+73C=	ENSP00000407473.2:n.363+73C=
ENST00000473257.3:c.234+73C=	ENSP00000501773.1:n.234+73C=
ENST00000477812.2:n.571-29C=
ENST00000484841.6:n.518-29C=
ENST00000493945.6:c.363+73C=	ENSP00000494269.1:n.363+73C=
ENST00000642480.2:c.363+73C=	ENSP00000495995.2:n.363+73C=
ENST00000645025.1:n.447-29C=
ENST00000645576.1:c.363+73C=	ENSP00000496101.1:n.363+73C=
ENST00000646664.1:c.363+73C= MANE Select	ENSP00000494750.1:n.363+73C=
ENST00000647275.1:c.-3-369C=	ENSP00000494185.1:n.-3-369C=
ENST00000674681.1:c.363+73C=	ENSP00000502821.1:n.363+73C=
ENST00000675515.1:c.363+73C=	ENSP00000501862.1:n.363+73C=
ENST00000676189.1:c.374+62C=	ENSP00000502538.1:n.374+62C=
ENST00000676319.1:c.87+483C=	ENSP00000502193.1:n.87+483C=
ENST00000676397.1:c.363+73C=	ENSP00000502286.1:n.363+73C=
ENST00000331789.9:c.363+73C=	ENSP00000349960.4:n.363+73C=
ENST00000425660.5:c.364-29C=	ENSP00000409264.1:n.364-29C=
ENST00000432588.5:c.363+73C=	ENSP00000407473.1:n.363+73C=
ENST00000462494.5:n.520C=
ENST00000473257.1:n.82-369C=
ENST00000477812.1:n.570+73C=
ENST00000480301.1:n.636C=
ENST00000484841.5:n.518+73C=
ENST00000493945.5:n.369+73C=
NM_001101.3:c.363+73C= , LRG_132t1:c.363+73C=	NP_001092.1:n.363+73C=
XM_006715764.1:c.-343-29C=	XP_006715827.1:n.-343-29C=
NM_001101.4:c.363+73C=	NP_001092.1:n.363+73C=
NM_001101.5:c.363+73C= MANE Select	NP_001092.1:n.363+73C=