Canonical Allele Identifier: CA2487053199
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762513A= , CM000663.2:g.236762513A= GRCh38
NC_000001.10:g.236925813A= , CM000663.1:g.236925813A= GRCh37
NC_000001.9:g.234992436A= NCBI36
NG_009081.1:g.81044A=
NG_009081.2:g.103373A=

Transcript Alleles

HGVS Amino-acid change
ENST00000542672.7:c.2579A= ENSP00000443495.1:p.Gln860=
ENST00000461367.2:n.875A=
ENST00000492634.7:n.2509A=
ENST00000682015.1:c.2486A= ENSP00000506961.1:p.Gln829=
ENST00000682490.1:n.497A=
ENST00000682692.1:n.3674A=
ENST00000682966.1:n.8220A=
ENST00000683111.1:c.*1865A= ENSP00000507913.1:n.*1865A=
ENST00000683322.1:n.3931A=
ENST00000683805.1:n.1370A=
ENST00000684050.1:n.5217A=
ENST00000684122.1:n.2013A=
ENST00000684286.1:n.4134A=
ENST00000684502.1:n.3876A=
ENST00000684763.1:n.1194A=
ENST00000366578.6:c.2579A= MANE Select ENSP00000355537.4:p.Gln860=
ENST00000492634.6:n.2509A=
ENST00000542672.6:c.2579A= ENSP00000443495.1:p.Gln860=
ENST00000651091.1:c.2269A= ENSP00000498677.1:n.2269A=
ENST00000651275.1:c.2471A= ENSP00000498926.1:p.Gln824=
ENST00000651781.1:c.1659A=
ENST00000651786.1:c.*1951A= ENSP00000498364.1:n.*1951A=
ENST00000652096.1:c.*1984A= ENSP00000498896.1:n.*1984A=
ENST00000366578.5:c.2579A= ENSP00000355537.4:p.Gln860=
ENST00000461367.1:n.788A=
ENST00000542672.5:c.2579A= ENSP00000443495.1:p.Gln860=
ENST00000546208.5:c.1955A= ENSP00000438384.2:p.Gln652=
NM_001103.3:c.2579A= NP_001094.1:p.Gln860=
NM_001278343.1:c.2579A= NP_001265272.1:p.Gln860=
NM_001278344.1:c.1955A= NP_001265273.1:p.Gln652=
NM_001278343.2:c.2579A= NP_001265272.1:p.Gln860=
NM_001103.4:c.2579A= MANE Select NP_001094.1:p.Gln860=
NM_001278344.2:c.1955A= NP_001265273.1:p.Gln652=