Canonical Allele Identifier: CA345392143

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925792A>G (hg19) ; chr1:g.236762492A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762492A>G , CM000663.2:g.236762492A>G	GRCh38
NC_000001.10:g.236925792A>G , CM000663.1:g.236925792A>G	GRCh37
NC_000001.9:g.234992415A>G	NCBI36
NG_009081.1:g.81023A>G
NG_009081.2:g.103352A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2558A>G	ENSP00000443495.1:p.Glu853Gly
ENST00000461367.2:n.854A>G
ENST00000492634.7:n.2488A>G
ENST00000682015.1:c.2465A>G	ENSP00000506961.1:p.Glu822Gly
ENST00000682490.1:n.476A>G
ENST00000682692.1:n.3653A>G
ENST00000682966.1:n.8199A>G
ENST00000683111.1:c.*1844A>G	ENSP00000507913.1:n.*1844A>G
ENST00000683322.1:n.3910A>G
ENST00000683805.1:n.1349A>G
ENST00000684050.1:n.5196A>G
ENST00000684122.1:n.1992A>G
ENST00000684286.1:n.4113A>G
ENST00000684502.1:n.3855A>G
ENST00000684763.1:n.1173A>G
ENST00000366578.6:c.2558A>G MANE Select	ENSP00000355537.4:p.Glu853Gly
ENST00000492634.6:n.2488A>G
ENST00000542672.6:c.2558A>G	ENSP00000443495.1:p.Glu853Gly
ENST00000651091.1:c.2248A>G	ENSP00000498677.1:n.2248A>G
ENST00000651275.1:c.2450A>G	ENSP00000498926.1:p.Glu817Gly
ENST00000651781.1:c.1638A>G
ENST00000651786.1:c.*1930A>G	ENSP00000498364.1:n.*1930A>G
ENST00000652096.1:c.*1963A>G	ENSP00000498896.1:n.*1963A>G
ENST00000366578.5:c.2558A>G	ENSP00000355537.4:p.Glu853Gly
ENST00000461367.1:n.767A>G
ENST00000542672.5:c.2558A>G	ENSP00000443495.1:p.Glu853Gly
ENST00000546208.5:c.1934A>G	ENSP00000438384.2:p.Glu645Gly
NM_001103.3:c.2558A>G	NP_001094.1:p.Glu853Gly
NM_001278343.1:c.2558A>G	NP_001265272.1:p.Glu853Gly
NM_001278344.1:c.1934A>G	NP_001265273.1:p.Glu645Gly
NM_001278343.2:c.2558A>G	NP_001265272.1:p.Glu853Gly
NM_001103.4:c.2558A>G MANE Select	NP_001094.1:p.Glu853Gly
NM_001278344.2:c.1934A>G	NP_001265273.1:p.Glu645Gly