Canonical Allele Identifier: CA2487053258

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762635A= , CM000663.2:g.236762635A=	GRCh38
NC_000001.10:g.236925935A= , CM000663.1:g.236925935A=	GRCh37
NC_000001.9:g.234992558A=	NCBI36
NG_009081.1:g.81166A=
NG_009081.2:g.103495A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.*16A=	ENSP00000443495.1:n.*16A=
ENST00000461367.2:n.997A=
ENST00000492634.7:n.2631A=
ENST00000682015.1:c.*16A=	ENSP00000506961.1:n.*16A=
ENST00000682490.1:n.619A=
ENST00000682692.1:n.3796A=
ENST00000682966.1:n.8342A=
ENST00000683111.1:c.*1987A=	ENSP00000507913.1:n.*1987A=
ENST00000683322.1:n.4053A=
ENST00000683805.1:n.1492A=
ENST00000684050.1:n.5339A=
ENST00000684122.1:n.2135A=
ENST00000684286.1:n.4256A=
ENST00000684502.1:n.3998A=
ENST00000684763.1:n.1316A=
ENST00000366578.6:c.*16A= MANE Select	ENSP00000355537.4:n.*16A=
ENST00000492634.6:n.2631A=
ENST00000542672.6:c.*16A=	ENSP00000443495.1:n.*16A=
ENST00000651275.1:c.2593A=	ENSP00000498926.1:n.2593A=
ENST00000651781.1:c.1781A=
ENST00000651786.1:c.*2073A=	ENSP00000498364.1:n.*2073A=
ENST00000652096.1:c.*2106A=	ENSP00000498896.1:n.*2106A=
ENST00000366578.5:c.*16A=	ENSP00000355537.4:n.*16A=
ENST00000542672.5:c.*16A=	ENSP00000443495.1:n.*16A=
ENST00000546208.5:c.*16A=	ENSP00000438384.2:n.*16A=
NM_001103.3:c.*16A=	NP_001094.1:n.*16A=
NM_001278343.1:c.*16A=	NP_001265272.1:n.*16A=
NM_001278344.1:c.*16A=	NP_001265273.1:n.*16A=
NM_001278343.2:c.*16A=	NP_001265272.1:n.*16A=
NM_001103.4:c.*16A= MANE Select	NP_001094.1:n.*16A=
NM_001278344.2:c.*16A=	NP_001265273.1:n.*16A=