Canonical Allele Identifier: CA2487050389

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755225G= , CM000663.2:g.236755225G=	GRCh38
NC_000001.10:g.236918525G= , CM000663.1:g.236918525G=	GRCh37
NC_000001.9:g.234985148G=	NCBI36
NG_009081.1:g.73756G=
NG_009081.2:g.96085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2154+27G=	ENSP00000443495.1:n.2154+27G=
ENST00000461367.2:n.450+27G=
ENST00000492634.7:n.2084+27G=
ENST00000682015.1:c.2061+27G=	ENSP00000506961.1:n.2061+27G=
ENST00000682692.1:n.3249+27G=
ENST00000682966.1:n.7795+27G=
ENST00000683111.1:c.*1440+27G=	ENSP00000507913.1:n.*1440+27G=
ENST00000683322.1:n.3506+27G=
ENST00000683805.1:n.945+27G=
ENST00000684050.1:n.4792+27G=
ENST00000684122.1:n.301+27G=
ENST00000684286.1:n.3709+27G=
ENST00000684502.1:n.3451+27G=
ENST00000684763.1:n.769+27G=
ENST00000366578.6:c.2154+27G= MANE Select	ENSP00000355537.4:n.2154+27G=
ENST00000492634.6:n.2084+27G=
ENST00000542672.6:c.2154+27G=	ENSP00000443495.1:n.2154+27G=
ENST00000651091.1:c.1844+27G=	ENSP00000498677.1:n.1844+27G=
ENST00000651275.1:c.2046+27G=	ENSP00000498926.1:n.2046+27G=
ENST00000651781.1:c.1234+27G=
ENST00000651786.1:c.*1526+27G=	ENSP00000498364.1:n.*1526+27G=
ENST00000652096.1:c.*1559+27G=	ENSP00000498896.1:n.*1559+27G=
ENST00000366578.5:c.2154+27G=	ENSP00000355537.4:n.2154+27G=
ENST00000461367.1:n.363+27G=
ENST00000542672.5:c.2154+27G=	ENSP00000443495.1:n.2154+27G=
ENST00000546208.5:c.1530+27G=	ENSP00000438384.2:n.1530+27G=
NM_001103.3:c.2154+27G=	NP_001094.1:n.2154+27G=
NM_001278343.1:c.2154+27G=	NP_001265272.1:n.2154+27G=
NM_001278344.1:c.1530+27G=	NP_001265273.1:n.1530+27G=
NM_001278343.2:c.2154+27G=	NP_001265272.1:n.2154+27G=
NM_001103.4:c.2154+27G= MANE Select	NP_001094.1:n.2154+27G=
NM_001278344.2:c.1530+27G=	NP_001265273.1:n.1530+27G=