Canonical Allele Identifier: CA2487053249

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762625A= , CM000663.2:g.236762625A=	GRCh38
NC_000001.10:g.236925925A= , CM000663.1:g.236925925A=	GRCh37
NC_000001.9:g.234992548A=	NCBI36
NG_009081.1:g.81156A=
NG_009081.2:g.103485A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000542672.7:c.*6A=	ENSP00000443495.1:n.*6A=
ENST00000461367.2:n.987A=
ENST00000492634.7:n.2621A=
ENST00000682015.1:c.*6A=	ENSP00000506961.1:n.*6A=
ENST00000682490.1:n.609A=
ENST00000682692.1:n.3786A=
ENST00000682966.1:n.8332A=
ENST00000683111.1:c.*1977A=	ENSP00000507913.1:n.*1977A=
ENST00000683322.1:n.4043A=
ENST00000683805.1:n.1482A=
ENST00000684050.1:n.5329A=
ENST00000684122.1:n.2125A=
ENST00000684286.1:n.4246A=
ENST00000684502.1:n.3988A=
ENST00000684763.1:n.1306A=
ENST00000366578.6:c.*6A= MANE Select	ENSP00000355537.4:n.*6A=
ENST00000492634.6:n.2621A=
ENST00000542672.6:c.*6A=	ENSP00000443495.1:n.*6A=
ENST00000651275.1:c.2583A=	ENSP00000498926.1:n.2583A=
ENST00000651781.1:c.1771A=
ENST00000651786.1:c.*2063A=	ENSP00000498364.1:n.*2063A=
ENST00000652096.1:c.*2096A=	ENSP00000498896.1:n.*2096A=
ENST00000366578.5:c.*6A=	ENSP00000355537.4:n.*6A=
ENST00000542672.5:c.*6A=	ENSP00000443495.1:n.*6A=
ENST00000546208.5:c.*6A=	ENSP00000438384.2:n.*6A=
NM_001103.3:c.*6A=	NP_001094.1:n.*6A=
NM_001278343.1:c.*6A=	NP_001265272.1:n.*6A=
NM_001278344.1:c.*6A=	NP_001265273.1:n.*6A=
NM_001278343.2:c.*6A=	NP_001265272.1:n.*6A=
NM_001103.4:c.*6A= MANE Select	NP_001094.1:n.*6A=
NM_001278344.2:c.*6A=	NP_001265273.1:n.*6A=