Canonical Allele Identifier: CA2487053206
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762532G= , CM000663.2:g.236762532G= GRCh38
NC_000001.10:g.236925832G= , CM000663.1:g.236925832G= GRCh37
NC_000001.9:g.234992455G= NCBI36
NG_009081.1:g.81063G=
NG_009081.2:g.103392G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2598G= ENSP00000443495.1:p.Met866=
ENST00000461367.2:n.894G=
ENST00000492634.7:n.2528G=
ENST00000682015.1:c.2505G= ENSP00000506961.1:p.Met835=
ENST00000682490.1:n.516G=
ENST00000682692.1:n.3693G=
ENST00000682966.1:n.8239G=
ENST00000683111.1:c.*1884G= ENSP00000507913.1:n.*1884G=
ENST00000683322.1:n.3950G=
ENST00000683805.1:n.1389G=
ENST00000684050.1:n.5236G=
ENST00000684122.1:n.2032G=
ENST00000684286.1:n.4153G=
ENST00000684502.1:n.3895G=
ENST00000684763.1:n.1213G=
ENST00000366578.6:c.2598G= MANE Select ENSP00000355537.4:p.Met866=
ENST00000492634.6:n.2528G=
ENST00000542672.6:c.2598G= ENSP00000443495.1:p.Met866=
ENST00000651091.1:c.2288G= ENSP00000498677.1:n.2288G=
ENST00000651275.1:c.2490G= ENSP00000498926.1:p.Met830=
ENST00000651781.1:c.1678G=
ENST00000651786.1:c.*1970G= ENSP00000498364.1:n.*1970G=
ENST00000652096.1:c.*2003G= ENSP00000498896.1:n.*2003G=
ENST00000366578.5:c.2598G= ENSP00000355537.4:p.Met866=
ENST00000461367.1:n.807G=
ENST00000542672.5:c.2598G= ENSP00000443495.1:p.Met866=
ENST00000546208.5:c.1974G= ENSP00000438384.2:p.Met658=
NM_001103.3:c.2598G= NP_001094.1:p.Met866=
NM_001278343.1:c.2598G= NP_001265272.1:p.Met866=
NM_001278344.1:c.1974G= NP_001265273.1:p.Met658=
NM_001278343.2:c.2598G= NP_001265272.1:p.Met866=
NM_001103.4:c.2598G= MANE Select NP_001094.1:p.Met866=
NM_001278344.2:c.1974G= NP_001265273.1:p.Met658=