Canonical Allele Identifier: CA1148009809
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236755095A= , CM000663.2:g.236755095A= GRCh38
NC_000001.10:g.236918395A= , CM000663.1:g.236918395A= GRCh37
NC_000001.9:g.234985018A= NCBI36
NG_009081.1:g.73626A=
NG_009081.2:g.95955A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2051A= ENSP00000443495.1:p.Asn684=
ENST00000461367.2:n.347A=
ENST00000492634.7:n.1981A=
ENST00000682015.1:c.1958A= ENSP00000506961.1:p.Asn653=
ENST00000682692.1:n.3146A=
ENST00000682966.1:n.7692A=
ENST00000683111.1:c.*1337A= ENSP00000507913.1:n.*1337A=
ENST00000683322.1:n.3403A=
ENST00000683805.1:n.842A=
ENST00000684050.1:n.4689A=
ENST00000684122.1:n.198A=
ENST00000684286.1:n.3606A=
ENST00000684502.1:n.3348A=
ENST00000684763.1:n.666A=
ENST00000366578.6:c.2051A= MANE Select ENSP00000355537.4:p.Asn684=
ENST00000492634.6:n.1981A=
ENST00000542672.6:c.2051A= ENSP00000443495.1:p.Asn684=
ENST00000651091.1:c.1741A= ENSP00000498677.1:n.1741A=
ENST00000651275.1:c.1943A= ENSP00000498926.1:p.Asn648=
ENST00000651781.1:c.1131A=
ENST00000651786.1:c.*1423A= ENSP00000498364.1:n.*1423A=
ENST00000652096.1:c.*1456A= ENSP00000498896.1:n.*1456A=
ENST00000366578.5:c.2051A= ENSP00000355537.4:p.Asn684=
ENST00000461367.1:n.260A=
ENST00000542672.5:c.2051A= ENSP00000443495.1:p.Asn684=
ENST00000546208.5:c.1427A= ENSP00000438384.2:p.Asn476=
NM_001103.3:c.2051A= NP_001094.1:p.Asn684=
NM_001278343.1:c.2051A= NP_001265272.1:p.Asn684=
NM_001278344.1:c.1427A= NP_001265273.1:p.Asn476=
NM_001278343.2:c.2051A= NP_001265272.1:p.Asn684=
NM_001103.4:c.2051A= MANE Select NP_001094.1:p.Asn684=
NM_001278344.2:c.1427A= NP_001265273.1:p.Asn476=