Canonical Allele Identifier: CA2487053224
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762564G= , CM000663.2:g.236762564G= GRCh38
NC_000001.10:g.236925864G= , CM000663.1:g.236925864G= GRCh37
NC_000001.9:g.234992487G= NCBI36
NG_009081.1:g.81095G=
NG_009081.2:g.103424G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2630G= ENSP00000443495.1:p.Gly877=
ENST00000461367.2:n.926G=
ENST00000492634.7:n.2560G=
ENST00000682015.1:c.2537G= ENSP00000506961.1:p.Gly846=
ENST00000682490.1:n.548G=
ENST00000682692.1:n.3725G=
ENST00000682966.1:n.8271G=
ENST00000683111.1:c.*1916G= ENSP00000507913.1:n.*1916G=
ENST00000683322.1:n.3982G=
ENST00000683805.1:n.1421G=
ENST00000684050.1:n.5268G=
ENST00000684122.1:n.2064G=
ENST00000684286.1:n.4185G=
ENST00000684502.1:n.3927G=
ENST00000684763.1:n.1245G=
ENST00000366578.6:c.2630G= MANE Select ENSP00000355537.4:p.Gly877=
ENST00000492634.6:n.2560G=
ENST00000542672.6:c.2630G= ENSP00000443495.1:p.Gly877=
ENST00000651091.1:c.2320G= ENSP00000498677.1:n.2320G=
ENST00000651275.1:c.2522G= ENSP00000498926.1:p.Gly841=
ENST00000651781.1:c.1710G=
ENST00000651786.1:c.*2002G= ENSP00000498364.1:n.*2002G=
ENST00000652096.1:c.*2035G= ENSP00000498896.1:n.*2035G=
ENST00000366578.5:c.2630G= ENSP00000355537.4:p.Gly877=
ENST00000461367.1:n.839G=
ENST00000542672.5:c.2630G= ENSP00000443495.1:p.Gly877=
ENST00000546208.5:c.2006G= ENSP00000438384.2:p.Gly669=
NM_001103.3:c.2630G= NP_001094.1:p.Gly877=
NM_001278343.1:c.2630G= NP_001265272.1:p.Gly877=
NM_001278344.1:c.2006G= NP_001265273.1:p.Gly669=
NM_001278343.2:c.2630G= NP_001265272.1:p.Gly877=
NM_001103.4:c.2630G= MANE Select NP_001094.1:p.Gly877=
NM_001278344.2:c.2006G= NP_001265273.1:p.Gly669=