Canonical Allele Identifier: CA1140326534
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762544G= , CM000663.2:g.236762544G= GRCh38
NC_000001.10:g.236925844G= , CM000663.1:g.236925844G= GRCh37
NC_000001.9:g.234992467G= NCBI36
NG_009081.1:g.81075G=
NG_009081.2:g.103404G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2610G= ENSP00000443495.1:p.Ser870=
ENST00000461367.2:n.906G=
ENST00000492634.7:n.2540G=
ENST00000682015.1:c.2517G= ENSP00000506961.1:p.Ser839=
ENST00000682490.1:n.528G=
ENST00000682692.1:n.3705G=
ENST00000682966.1:n.8251G=
ENST00000683111.1:c.*1896G= ENSP00000507913.1:n.*1896G=
ENST00000683322.1:n.3962G=
ENST00000683805.1:n.1401G=
ENST00000684050.1:n.5248G=
ENST00000684122.1:n.2044G=
ENST00000684286.1:n.4165G=
ENST00000684502.1:n.3907G=
ENST00000684763.1:n.1225G=
ENST00000366578.6:c.2610G= MANE Select ENSP00000355537.4:p.Ser870=
ENST00000492634.6:n.2540G=
ENST00000542672.6:c.2610G= ENSP00000443495.1:p.Ser870=
ENST00000651091.1:c.2300G= ENSP00000498677.1:n.2300G=
ENST00000651275.1:c.2502G= ENSP00000498926.1:p.Ser834=
ENST00000651781.1:c.1690G=
ENST00000651786.1:c.*1982G= ENSP00000498364.1:n.*1982G=
ENST00000652096.1:c.*2015G= ENSP00000498896.1:n.*2015G=
ENST00000366578.5:c.2610G= ENSP00000355537.4:p.Ser870=
ENST00000461367.1:n.819G=
ENST00000542672.5:c.2610G= ENSP00000443495.1:p.Ser870=
ENST00000546208.5:c.1986G= ENSP00000438384.2:p.Ser662=
NM_001103.3:c.2610G= NP_001094.1:p.Ser870=
NM_001278343.1:c.2610G= NP_001265272.1:p.Ser870=
NM_001278344.1:c.1986G= NP_001265273.1:p.Ser662=
NM_001278343.2:c.2610G= NP_001265272.1:p.Ser870=
NM_001103.4:c.2610G= MANE Select NP_001094.1:p.Ser870=
NM_001278344.2:c.1986G= NP_001265273.1:p.Ser662=