Canonical Allele Identifier: CA423811275

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925907G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762607G>A , CM000663.2:g.236762607G>A	GRCh38
NC_000001.10:g.236925907G>A , CM000663.1:g.236925907G>A	GRCh37
NC_000001.9:g.234992530G>A	NCBI36
NG_009081.1:g.81138G>A
NG_009081.2:g.103467G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2673G>A	ENSP00000443495.1:p.Glu891=
ENST00000461367.2:n.969G>A
ENST00000492634.7:n.2603G>A
ENST00000682015.1:c.2580G>A	ENSP00000506961.1:p.Glu860=
ENST00000682490.1:n.591G>A
ENST00000682692.1:n.3768G>A
ENST00000682966.1:n.8314G>A
ENST00000683111.1:c.*1959G>A	ENSP00000507913.1:n.*1959G>A
ENST00000683322.1:n.4025G>A
ENST00000683805.1:n.1464G>A
ENST00000684050.1:n.5311G>A
ENST00000684122.1:n.2107G>A
ENST00000684286.1:n.4228G>A
ENST00000684502.1:n.3970G>A
ENST00000684763.1:n.1288G>A
ENST00000366578.6:c.2673G>A MANE Select	ENSP00000355537.4:p.Glu891=
ENST00000492634.6:n.2603G>A
ENST00000542672.6:c.2673G>A	ENSP00000443495.1:p.Glu891=
ENST00000651275.1:c.2565G>A	ENSP00000498926.1:p.Glu855=
ENST00000651781.1:c.1753G>A
ENST00000651786.1:c.*2045G>A	ENSP00000498364.1:n.*2045G>A
ENST00000652096.1:c.*2078G>A	ENSP00000498896.1:n.*2078G>A
ENST00000366578.5:c.2673G>A	ENSP00000355537.4:p.Glu891=
ENST00000542672.5:c.2673G>A	ENSP00000443495.1:p.Glu891=
ENST00000546208.5:c.2049G>A	ENSP00000438384.2:p.Glu683=
NM_001103.3:c.2673G>A	NP_001094.1:p.Glu891=
NM_001278343.1:c.2673G>A	NP_001265272.1:p.Glu891=
NM_001278344.1:c.2049G>A	NP_001265273.1:p.Glu683=
NM_001278343.2:c.2673G>A	NP_001265272.1:p.Glu891=
NM_001103.4:c.2673G>A MANE Select	NP_001094.1:p.Glu891=
NM_001278344.2:c.2049G>A	NP_001265273.1:p.Glu683=