Canonical Allele Identifier: CA1684975832

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528605T= , CM000669.2:g.5528605T=	GRCh38
NC_000007.13:g.5568236T= , CM000669.1:g.5568236T=	GRCh37
NC_000007.12:g.5534762T=	NCBI36
NG_007992.1:g.6997A= , LRG_132:g.6997A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.478A=	ENSP00000407473.2:p.Thr160=
ENST00000473257.3:c.349A=	ENSP00000501773.1:p.Thr117=
ENST00000477812.2:n.1025A=
ENST00000493945.6:c.478A=	ENSP00000494269.1:p.Thr160=
ENST00000642480.2:c.478A=	ENSP00000495995.2:p.Thr160=
ENST00000645576.1:c.430A=	ENSP00000496101.1:p.Thr144=
ENST00000646664.1:c.478A= MANE Select	ENSP00000494750.1:p.Thr160=
ENST00000647275.1:c.112A=	ENSP00000494185.1:p.Thr38=
ENST00000674681.1:c.478A=	ENSP00000502821.1:p.Thr160=
ENST00000675515.1:c.478A=	ENSP00000501862.1:p.Thr160=
ENST00000676189.1:c.*21A=	ENSP00000502538.1:n.*21A=
ENST00000676319.1:c.88-822A=	ENSP00000502193.1:n.88-822A=
ENST00000676397.1:c.478A=	ENSP00000502286.1:p.Thr160=
ENST00000331789.9:c.478A=	ENSP00000349960.4:p.Thr160=
ENST00000425660.5:c.*141A=	ENSP00000409264.1:n.*141A=
ENST00000432588.5:c.478A=	ENSP00000407473.1:p.Thr160=
ENST00000462494.5:n.1003A=
ENST00000473257.1:n.196A=
ENST00000477812.1:n.685A=
ENST00000484841.5:n.633A=
ENST00000493945.5:n.484A=
NM_001101.3:c.478A= , LRG_132t1:c.478A=	NP_001092.1:p.Thr160=
XM_006715764.1:c.112A=	XP_006715827.1:p.Thr38=
NM_001101.4:c.478A=	NP_001092.1:p.Thr160=
NM_001101.5:c.478A= MANE Select	NP_001092.1:p.Thr160=