Canonical Allele Identifier: CA2487053276

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762687G= , CM000663.2:g.236762687G=	GRCh38
NC_000001.10:g.236925987G= , CM000663.1:g.236925987G=	GRCh37
NC_000001.9:g.234992610G=	NCBI36
NG_009081.1:g.81218G=
NG_009081.2:g.103547G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.*68G=	ENSP00000443495.1:n.*68G=
ENST00000461367.2:n.1049G=
ENST00000492634.7:n.2683G=
ENST00000682015.1:c.*68G=	ENSP00000506961.1:n.*68G=
ENST00000682490.1:n.671G=
ENST00000682692.1:n.3848G=
ENST00000682966.1:n.8394G=
ENST00000683111.1:c.*2039G=	ENSP00000507913.1:n.*2039G=
ENST00000683322.1:n.4105G=
ENST00000683805.1:n.1544G=
ENST00000684050.1:n.5391G=
ENST00000684122.1:n.2187G=
ENST00000684286.1:n.4308G=
ENST00000684502.1:n.4050G=
ENST00000684763.1:n.1368G=
ENST00000366578.6:c.*68G= MANE Select	ENSP00000355537.4:n.*68G=
ENST00000492634.6:n.2683G=
ENST00000542672.6:c.*68G=	ENSP00000443495.1:n.*68G=
ENST00000651275.1:c.2645G=	ENSP00000498926.1:n.2645G=
ENST00000651781.1:c.1833G=
ENST00000651786.1:c.*2125G=	ENSP00000498364.1:n.*2125G=
ENST00000652096.1:c.*2158G=	ENSP00000498896.1:n.*2158G=
ENST00000366578.5:c.*68G=	ENSP00000355537.4:n.*68G=
ENST00000542672.5:c.*68G=	ENSP00000443495.1:n.*68G=
ENST00000546208.5:c.*68G=	ENSP00000438384.2:n.*68G=
NM_001103.3:c.*68G=	NP_001094.1:n.*68G=
NM_001278343.1:c.*68G=	NP_001265272.1:n.*68G=
NM_001278344.1:c.*68G=	NP_001265273.1:n.*68G=
NM_001278343.2:c.*68G=	NP_001265272.1:n.*68G=
NM_001103.4:c.*68G= MANE Select	NP_001094.1:n.*68G=
NM_001278344.2:c.*68G=	NP_001265273.1:n.*68G=