Canonical Allele Identifier: CA345392703

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925906A>T (hg19) ; chr1:g.236762606A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762606A>T , CM000663.2:g.236762606A>T	GRCh38
NC_000001.10:g.236925906A>T , CM000663.1:g.236925906A>T	GRCh37
NC_000001.9:g.234992529A>T	NCBI36
NG_009081.1:g.81137A>T
NG_009081.2:g.103466A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2672A>T	ENSP00000443495.1:p.Glu891Val
ENST00000461367.2:n.968A>T
ENST00000492634.7:n.2602A>T
ENST00000682015.1:c.2579A>T	ENSP00000506961.1:p.Glu860Val
ENST00000682490.1:n.590A>T
ENST00000682692.1:n.3767A>T
ENST00000682966.1:n.8313A>T
ENST00000683111.1:c.*1958A>T	ENSP00000507913.1:n.*1958A>T
ENST00000683322.1:n.4024A>T
ENST00000683805.1:n.1463A>T
ENST00000684050.1:n.5310A>T
ENST00000684122.1:n.2106A>T
ENST00000684286.1:n.4227A>T
ENST00000684502.1:n.3969A>T
ENST00000684763.1:n.1287A>T
ENST00000366578.6:c.2672A>T MANE Select	ENSP00000355537.4:p.Glu891Val
ENST00000492634.6:n.2602A>T
ENST00000542672.6:c.2672A>T	ENSP00000443495.1:p.Glu891Val
ENST00000651275.1:c.2564A>T	ENSP00000498926.1:p.Glu855Val
ENST00000651781.1:c.1752A>T
ENST00000651786.1:c.*2044A>T	ENSP00000498364.1:n.*2044A>T
ENST00000652096.1:c.*2077A>T	ENSP00000498896.1:n.*2077A>T
ENST00000366578.5:c.2672A>T	ENSP00000355537.4:p.Glu891Val
ENST00000542672.5:c.2672A>T	ENSP00000443495.1:p.Glu891Val
ENST00000546208.5:c.2048A>T	ENSP00000438384.2:p.Glu683Val
NM_001103.3:c.2672A>T	NP_001094.1:p.Glu891Val
NM_001278343.1:c.2672A>T	NP_001265272.1:p.Glu891Val
NM_001278344.1:c.2048A>T	NP_001265273.1:p.Glu683Val
NM_001278343.2:c.2672A>T	NP_001265272.1:p.Glu891Val
NM_001103.4:c.2672A>T MANE Select	NP_001094.1:p.Glu891Val
NM_001278344.2:c.2048A>T	NP_001265273.1:p.Glu683Val