Canonical Allele Identifier: CA2487053209
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762537C= , CM000663.2:g.236762537C= GRCh38
NC_000001.10:g.236925837C= , CM000663.1:g.236925837C= GRCh37
NC_000001.9:g.234992460C= NCBI36
NG_009081.1:g.81068C=
NG_009081.2:g.103397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2603C= ENSP00000443495.1:p.Ala868=
ENST00000461367.2:n.899C=
ENST00000492634.7:n.2533C=
ENST00000682015.1:c.2510C= ENSP00000506961.1:p.Ala837=
ENST00000682490.1:n.521C=
ENST00000682692.1:n.3698C=
ENST00000682966.1:n.8244C=
ENST00000683111.1:c.*1889C= ENSP00000507913.1:n.*1889C=
ENST00000683322.1:n.3955C=
ENST00000683805.1:n.1394C=
ENST00000684050.1:n.5241C=
ENST00000684122.1:n.2037C=
ENST00000684286.1:n.4158C=
ENST00000684502.1:n.3900C=
ENST00000684763.1:n.1218C=
ENST00000366578.6:c.2603C= MANE Select ENSP00000355537.4:p.Ala868=
ENST00000492634.6:n.2533C=
ENST00000542672.6:c.2603C= ENSP00000443495.1:p.Ala868=
ENST00000651091.1:c.2293C= ENSP00000498677.1:n.2293C=
ENST00000651275.1:c.2495C= ENSP00000498926.1:p.Ala832=
ENST00000651781.1:c.1683C=
ENST00000651786.1:c.*1975C= ENSP00000498364.1:n.*1975C=
ENST00000652096.1:c.*2008C= ENSP00000498896.1:n.*2008C=
ENST00000366578.5:c.2603C= ENSP00000355537.4:p.Ala868=
ENST00000461367.1:n.812C=
ENST00000542672.5:c.2603C= ENSP00000443495.1:p.Ala868=
ENST00000546208.5:c.1979C= ENSP00000438384.2:p.Ala660=
NM_001103.3:c.2603C= NP_001094.1:p.Ala868=
NM_001278343.1:c.2603C= NP_001265272.1:p.Ala868=
NM_001278344.1:c.1979C= NP_001265273.1:p.Ala660=
NM_001278343.2:c.2603C= NP_001265272.1:p.Ala868=
NM_001103.4:c.2603C= MANE Select NP_001094.1:p.Ala868=
NM_001278344.2:c.1979C= NP_001265273.1:p.Ala660=