Canonical Allele Identifier: CA2487053197
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762510C= , CM000663.2:g.236762510C= GRCh38
NC_000001.10:g.236925810C= , CM000663.1:g.236925810C= GRCh37
NC_000001.9:g.234992433C= NCBI36
NG_009081.1:g.81041C=
NG_009081.2:g.103370C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2576C= ENSP00000443495.1:p.Ala859=
ENST00000461367.2:n.872C=
ENST00000492634.7:n.2506C=
ENST00000682015.1:c.2483C= ENSP00000506961.1:p.Ala828=
ENST00000682490.1:n.494C=
ENST00000682692.1:n.3671C=
ENST00000682966.1:n.8217C=
ENST00000683111.1:c.*1862C= ENSP00000507913.1:n.*1862C=
ENST00000683322.1:n.3928C=
ENST00000683805.1:n.1367C=
ENST00000684050.1:n.5214C=
ENST00000684122.1:n.2010C=
ENST00000684286.1:n.4131C=
ENST00000684502.1:n.3873C=
ENST00000684763.1:n.1191C=
ENST00000366578.6:c.2576C= MANE Select ENSP00000355537.4:p.Ala859=
ENST00000492634.6:n.2506C=
ENST00000542672.6:c.2576C= ENSP00000443495.1:p.Ala859=
ENST00000651091.1:c.2266C= ENSP00000498677.1:n.2266C=
ENST00000651275.1:c.2468C= ENSP00000498926.1:p.Ala823=
ENST00000651781.1:c.1656C=
ENST00000651786.1:c.*1948C= ENSP00000498364.1:n.*1948C=
ENST00000652096.1:c.*1981C= ENSP00000498896.1:n.*1981C=
ENST00000366578.5:c.2576C= ENSP00000355537.4:p.Ala859=
ENST00000461367.1:n.785C=
ENST00000542672.5:c.2576C= ENSP00000443495.1:p.Ala859=
ENST00000546208.5:c.1952C= ENSP00000438384.2:p.Ala651=
NM_001103.3:c.2576C= NP_001094.1:p.Ala859=
NM_001278343.1:c.2576C= NP_001265272.1:p.Ala859=
NM_001278344.1:c.1952C= NP_001265273.1:p.Ala651=
NM_001278343.2:c.2576C= NP_001265272.1:p.Ala859=
NM_001103.4:c.2576C= MANE Select NP_001094.1:p.Ala859=
NM_001278344.2:c.1952C= NP_001265273.1:p.Ala651=