Canonical Allele Identifier: CA2487053147

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762394G= , CM000663.2:g.236762394G=	GRCh38
NC_000001.10:g.236925694G= , CM000663.1:g.236925694G=	GRCh37
NC_000001.9:g.234992317G=	NCBI36
NG_009081.1:g.80925G=
NG_009081.2:g.103254G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2527-67G=	ENSP00000443495.1:n.2527-67G=
ENST00000461367.2:n.823-67G=
ENST00000492634.7:n.2457-67G=
ENST00000682015.1:c.2434-67G=	ENSP00000506961.1:n.2434-67G=
ENST00000682490.1:n.445-67G=
ENST00000682692.1:n.3622-67G=
ENST00000682966.1:n.8168-67G=
ENST00000683111.1:c.*1813-67G=	ENSP00000507913.1:n.*1813-67G=
ENST00000683322.1:n.3879-67G=
ENST00000683805.1:n.1318-67G=
ENST00000684050.1:n.5165-67G=
ENST00000684122.1:n.1894G=
ENST00000684286.1:n.4082-67G=
ENST00000684502.1:n.3824-67G=
ENST00000684763.1:n.1142-67G=
ENST00000366578.6:c.2527-67G= MANE Select	ENSP00000355537.4:n.2527-67G=
ENST00000492634.6:n.2457-67G=
ENST00000542672.6:c.2527-67G=	ENSP00000443495.1:n.2527-67G=
ENST00000651091.1:c.2217-67G=	ENSP00000498677.1:n.2217-67G=
ENST00000651275.1:c.2419-67G=	ENSP00000498926.1:n.2419-67G=
ENST00000651781.1:c.1607-67G=
ENST00000651786.1:c.*1899-67G=	ENSP00000498364.1:n.*1899-67G=
ENST00000652096.1:c.*1932-67G=	ENSP00000498896.1:n.*1932-67G=
ENST00000366578.5:c.2527-67G=	ENSP00000355537.4:n.2527-67G=
ENST00000461367.1:n.736-67G=
ENST00000542672.5:c.2527-67G=	ENSP00000443495.1:n.2527-67G=
ENST00000546208.5:c.1903-67G=	ENSP00000438384.2:n.1903-67G=
NM_001103.3:c.2527-67G=	NP_001094.1:n.2527-67G=
NM_001278343.1:c.2527-67G=	NP_001265272.1:n.2527-67G=
NM_001278344.1:c.1903-67G=	NP_001265273.1:n.1903-67G=
NM_001278343.2:c.2527-67G=	NP_001265272.1:n.2527-67G=
NM_001103.4:c.2527-67G= MANE Select	NP_001094.1:n.2527-67G=
NM_001278344.2:c.1903-67G=	NP_001265273.1:n.1903-67G=