Canonical Allele Identifier: CA2487053201
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762519G= , CM000663.2:g.236762519G= GRCh38
NC_000001.10:g.236925819G= , CM000663.1:g.236925819G= GRCh37
NC_000001.9:g.234992442G= NCBI36
NG_009081.1:g.81050G=
NG_009081.2:g.103379G=

Transcript Alleles

HGVS Amino-acid change
ENST00000542672.7:c.2585G= ENSP00000443495.1:p.Cys862=
ENST00000461367.2:n.881G=
ENST00000492634.7:n.2515G=
ENST00000682015.1:c.2492G= ENSP00000506961.1:p.Cys831=
ENST00000682490.1:n.503G=
ENST00000682692.1:n.3680G=
ENST00000682966.1:n.8226G=
ENST00000683111.1:c.*1871G= ENSP00000507913.1:n.*1871G=
ENST00000683322.1:n.3937G=
ENST00000683805.1:n.1376G=
ENST00000684050.1:n.5223G=
ENST00000684122.1:n.2019G=
ENST00000684286.1:n.4140G=
ENST00000684502.1:n.3882G=
ENST00000684763.1:n.1200G=
ENST00000366578.6:c.2585G= MANE Select ENSP00000355537.4:p.Cys862=
ENST00000492634.6:n.2515G=
ENST00000542672.6:c.2585G= ENSP00000443495.1:p.Cys862=
ENST00000651091.1:c.2275G= ENSP00000498677.1:n.2275G=
ENST00000651275.1:c.2477G= ENSP00000498926.1:p.Cys826=
ENST00000651781.1:c.1665G=
ENST00000651786.1:c.*1957G= ENSP00000498364.1:n.*1957G=
ENST00000652096.1:c.*1990G= ENSP00000498896.1:n.*1990G=
ENST00000366578.5:c.2585G= ENSP00000355537.4:p.Cys862=
ENST00000461367.1:n.794G=
ENST00000542672.5:c.2585G= ENSP00000443495.1:p.Cys862=
ENST00000546208.5:c.1961G= ENSP00000438384.2:p.Cys654=
NM_001103.3:c.2585G= NP_001094.1:p.Cys862=
NM_001278343.1:c.2585G= NP_001265272.1:p.Cys862=
NM_001278344.1:c.1961G= NP_001265273.1:p.Cys654=
NM_001278343.2:c.2585G= NP_001265272.1:p.Cys862=
NM_001103.4:c.2585G= MANE Select NP_001094.1:p.Cys862=
NM_001278344.2:c.1961G= NP_001265273.1:p.Cys654=