Canonical Allele Identifier: CA1143723206

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762546G= , CM000663.2:g.236762546G=	GRCh38
NC_000001.10:g.236925846G= , CM000663.1:g.236925846G=	GRCh37
NC_000001.9:g.234992469G=	NCBI36
NG_009081.1:g.81077G=
NG_009081.2:g.103406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2612G=	ENSP00000443495.1:p.Gly871=
ENST00000461367.2:n.908G=
ENST00000492634.7:n.2542G=
ENST00000682015.1:c.2519G=	ENSP00000506961.1:p.Gly840=
ENST00000682490.1:n.530G=
ENST00000682692.1:n.3707G=
ENST00000682966.1:n.8253G=
ENST00000683111.1:c.*1898G=	ENSP00000507913.1:n.*1898G=
ENST00000683322.1:n.3964G=
ENST00000683805.1:n.1403G=
ENST00000684050.1:n.5250G=
ENST00000684122.1:n.2046G=
ENST00000684286.1:n.4167G=
ENST00000684502.1:n.3909G=
ENST00000684763.1:n.1227G=
ENST00000366578.6:c.2612G= MANE Select	ENSP00000355537.4:p.Gly871=
ENST00000492634.6:n.2542G=
ENST00000542672.6:c.2612G=	ENSP00000443495.1:p.Gly871=
ENST00000651091.1:c.2302G=	ENSP00000498677.1:n.2302G=
ENST00000651275.1:c.2504G=	ENSP00000498926.1:p.Gly835=
ENST00000651781.1:c.1692G=
ENST00000651786.1:c.*1984G=	ENSP00000498364.1:n.*1984G=
ENST00000652096.1:c.*2017G=	ENSP00000498896.1:n.*2017G=
ENST00000366578.5:c.2612G=	ENSP00000355537.4:p.Gly871=
ENST00000461367.1:n.821G=
ENST00000542672.5:c.2612G=	ENSP00000443495.1:p.Gly871=
ENST00000546208.5:c.1988G=	ENSP00000438384.2:p.Gly663=
NM_001103.3:c.2612G=	NP_001094.1:p.Gly871=
NM_001278343.1:c.2612G=	NP_001265272.1:p.Gly871=
NM_001278344.1:c.1988G=	NP_001265273.1:p.Gly663=
NM_001278343.2:c.2612G=	NP_001265272.1:p.Gly871=
NM_001103.4:c.2612G= MANE Select	NP_001094.1:p.Gly871=
NM_001278344.2:c.1988G=	NP_001265273.1:p.Gly663=