Canonical Allele Identifier: CA2487053251

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762627C= , CM000663.2:g.236762627C=	GRCh38
NC_000001.10:g.236925927C= , CM000663.1:g.236925927C=	GRCh37
NC_000001.9:g.234992550C=	NCBI36
NG_009081.1:g.81158C=
NG_009081.2:g.103487C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.*8C=	ENSP00000443495.1:n.*8C=
ENST00000461367.2:n.989C=
ENST00000492634.7:n.2623C=
ENST00000682015.1:c.*8C=	ENSP00000506961.1:n.*8C=
ENST00000682490.1:n.611C=
ENST00000682692.1:n.3788C=
ENST00000682966.1:n.8334C=
ENST00000683111.1:c.*1979C=	ENSP00000507913.1:n.*1979C=
ENST00000683322.1:n.4045C=
ENST00000683805.1:n.1484C=
ENST00000684050.1:n.5331C=
ENST00000684122.1:n.2127C=
ENST00000684286.1:n.4248C=
ENST00000684502.1:n.3990C=
ENST00000684763.1:n.1308C=
ENST00000366578.6:c.*8C= MANE Select	ENSP00000355537.4:n.*8C=
ENST00000492634.6:n.2623C=
ENST00000542672.6:c.*8C=	ENSP00000443495.1:n.*8C=
ENST00000651275.1:c.2585C=	ENSP00000498926.1:n.2585C=
ENST00000651781.1:c.1773C=
ENST00000651786.1:c.*2065C=	ENSP00000498364.1:n.*2065C=
ENST00000652096.1:c.*2098C=	ENSP00000498896.1:n.*2098C=
ENST00000366578.5:c.*8C=	ENSP00000355537.4:n.*8C=
ENST00000542672.5:c.*8C=	ENSP00000443495.1:n.*8C=
ENST00000546208.5:c.*8C=	ENSP00000438384.2:n.*8C=
NM_001103.3:c.*8C=	NP_001094.1:n.*8C=
NM_001278343.1:c.*8C=	NP_001265272.1:n.*8C=
NM_001278344.1:c.*8C=	NP_001265273.1:n.*8C=
NM_001278343.2:c.*8C=	NP_001265272.1:n.*8C=
NM_001103.4:c.*8C= MANE Select	NP_001094.1:n.*8C=
NM_001278344.2:c.*8C=	NP_001265273.1:n.*8C=