Canonical Allele Identifier: CA1143476019
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762486G= , CM000663.2:g.236762486G= GRCh38
NC_000001.10:g.236925786G= , CM000663.1:g.236925786G= GRCh37
NC_000001.9:g.234992409G= NCBI36
NG_009081.1:g.81017G=
NG_009081.2:g.103346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2552G= ENSP00000443495.1:p.Arg851=
ENST00000461367.2:n.848G=
ENST00000492634.7:n.2482G=
ENST00000682015.1:c.2459G= ENSP00000506961.1:p.Arg820=
ENST00000682490.1:n.470G=
ENST00000682692.1:n.3647G=
ENST00000682966.1:n.8193G=
ENST00000683111.1:c.*1838G= ENSP00000507913.1:n.*1838G=
ENST00000683322.1:n.3904G=
ENST00000683805.1:n.1343G=
ENST00000684050.1:n.5190G=
ENST00000684122.1:n.1986G=
ENST00000684286.1:n.4107G=
ENST00000684502.1:n.3849G=
ENST00000684763.1:n.1167G=
ENST00000366578.6:c.2552G= MANE Select ENSP00000355537.4:p.Arg851=
ENST00000492634.6:n.2482G=
ENST00000542672.6:c.2552G= ENSP00000443495.1:p.Arg851=
ENST00000651091.1:c.2242G= ENSP00000498677.1:n.2242G=
ENST00000651275.1:c.2444G= ENSP00000498926.1:p.Arg815=
ENST00000651781.1:c.1632G=
ENST00000651786.1:c.*1924G= ENSP00000498364.1:n.*1924G=
ENST00000652096.1:c.*1957G= ENSP00000498896.1:n.*1957G=
ENST00000366578.5:c.2552G= ENSP00000355537.4:p.Arg851=
ENST00000461367.1:n.761G=
ENST00000542672.5:c.2552G= ENSP00000443495.1:p.Arg851=
ENST00000546208.5:c.1928G= ENSP00000438384.2:p.Arg643=
NM_001103.3:c.2552G= NP_001094.1:p.Arg851=
NM_001278343.1:c.2552G= NP_001265272.1:p.Arg851=
NM_001278344.1:c.1928G= NP_001265273.1:p.Arg643=
NM_001278343.2:c.2552G= NP_001265272.1:p.Arg851=
NM_001103.4:c.2552G= MANE Select NP_001094.1:p.Arg851=
NM_001278344.2:c.1928G= NP_001265273.1:p.Arg643=