Canonical Allele Identifier: CA2487050399

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755249C= , CM000663.2:g.236755249C=	GRCh38
NC_000001.10:g.236918549C= , CM000663.1:g.236918549C=	GRCh37
NC_000001.9:g.234985172C=	NCBI36
NG_009081.1:g.73780C=
NG_009081.2:g.96109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2154+51C=	ENSP00000443495.1:n.2154+51C=
ENST00000461367.2:n.450+51C=
ENST00000492634.7:n.2084+51C=
ENST00000682015.1:c.2061+51C=	ENSP00000506961.1:n.2061+51C=
ENST00000682692.1:n.3249+51C=
ENST00000682966.1:n.7795+51C=
ENST00000683111.1:c.*1440+51C=	ENSP00000507913.1:n.*1440+51C=
ENST00000683322.1:n.3506+51C=
ENST00000683805.1:n.945+51C=
ENST00000684050.1:n.4792+51C=
ENST00000684122.1:n.301+51C=
ENST00000684286.1:n.3709+51C=
ENST00000684502.1:n.3451+51C=
ENST00000684763.1:n.769+51C=
ENST00000366578.6:c.2154+51C= MANE Select	ENSP00000355537.4:n.2154+51C=
ENST00000492634.6:n.2084+51C=
ENST00000542672.6:c.2154+51C=	ENSP00000443495.1:n.2154+51C=
ENST00000651091.1:c.1844+51C=	ENSP00000498677.1:n.1844+51C=
ENST00000651275.1:c.2046+51C=	ENSP00000498926.1:n.2046+51C=
ENST00000651781.1:c.1234+51C=
ENST00000651786.1:c.*1526+51C=	ENSP00000498364.1:n.*1526+51C=
ENST00000652096.1:c.*1559+51C=	ENSP00000498896.1:n.*1559+51C=
ENST00000366578.5:c.2154+51C=	ENSP00000355537.4:n.2154+51C=
ENST00000461367.1:n.363+51C=
ENST00000542672.5:c.2154+51C=	ENSP00000443495.1:n.2154+51C=
ENST00000546208.5:c.1530+51C=	ENSP00000438384.2:n.1530+51C=
NM_001103.3:c.2154+51C=	NP_001094.1:n.2154+51C=
NM_001278343.1:c.2154+51C=	NP_001265272.1:n.2154+51C=
NM_001278344.1:c.1530+51C=	NP_001265273.1:n.1530+51C=
NM_001278343.2:c.2154+51C=	NP_001265272.1:n.2154+51C=
NM_001103.4:c.2154+51C= MANE Select	NP_001094.1:n.2154+51C=
NM_001278344.2:c.1530+51C=	NP_001265273.1:n.1530+51C=