Canonical Allele Identifier: CA1143355688

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755191C= , CM000663.2:g.236755191C=	GRCh38
NC_000001.10:g.236918491C= , CM000663.1:g.236918491C=	GRCh37
NC_000001.9:g.234985114C=	NCBI36
NG_009081.1:g.73722C=
NG_009081.2:g.96051C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000542672.7:c.2147C=	ENSP00000443495.1:p.Thr716=
ENST00000461367.2:n.443C=
ENST00000492634.7:n.2077C=
ENST00000682015.1:c.2054C=	ENSP00000506961.1:p.Thr685=
ENST00000682692.1:n.3242C=
ENST00000682966.1:n.7788C=
ENST00000683111.1:c.*1433C=	ENSP00000507913.1:n.*1433C=
ENST00000683322.1:n.3499C=
ENST00000683805.1:n.938C=
ENST00000684050.1:n.4785C=
ENST00000684122.1:n.294C=
ENST00000684286.1:n.3702C=
ENST00000684502.1:n.3444C=
ENST00000684763.1:n.762C=
ENST00000366578.6:c.2147C= MANE Select	ENSP00000355537.4:p.Thr716=
ENST00000492634.6:n.2077C=
ENST00000542672.6:c.2147C=	ENSP00000443495.1:p.Thr716=
ENST00000651091.1:c.1837C=	ENSP00000498677.1:n.1837C=
ENST00000651275.1:c.2039C=	ENSP00000498926.1:p.Thr680=
ENST00000651781.1:c.1227C=
ENST00000651786.1:c.*1519C=	ENSP00000498364.1:n.*1519C=
ENST00000652096.1:c.*1552C=	ENSP00000498896.1:n.*1552C=
ENST00000366578.5:c.2147C=	ENSP00000355537.4:p.Thr716=
ENST00000461367.1:n.356C=
ENST00000542672.5:c.2147C=	ENSP00000443495.1:p.Thr716=
ENST00000546208.5:c.1523C=	ENSP00000438384.2:p.Thr508=
NM_001103.3:c.2147C=	NP_001094.1:p.Thr716=
NM_001278343.1:c.2147C=	NP_001265272.1:p.Thr716=
NM_001278344.1:c.1523C=	NP_001265273.1:p.Thr508=
NM_001278343.2:c.2147C=	NP_001265272.1:p.Thr716=
NM_001103.4:c.2147C= MANE Select	NP_001094.1:p.Thr716=
NM_001278344.2:c.1523C=	NP_001265273.1:p.Thr508=