Canonical Allele Identifier: CA2487050341
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236755103A= , CM000663.2:g.236755103A= GRCh38
NC_000001.10:g.236918403A= , CM000663.1:g.236918403A= GRCh37
NC_000001.9:g.234985026A= NCBI36
NG_009081.1:g.73634A=
NG_009081.2:g.95963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2059A= ENSP00000443495.1:p.Asn687=
ENST00000461367.2:n.355A=
ENST00000492634.7:n.1989A=
ENST00000682015.1:c.1966A= ENSP00000506961.1:p.Asn656=
ENST00000682692.1:n.3154A=
ENST00000682966.1:n.7700A=
ENST00000683111.1:c.*1345A= ENSP00000507913.1:n.*1345A=
ENST00000683322.1:n.3411A=
ENST00000683805.1:n.850A=
ENST00000684050.1:n.4697A=
ENST00000684122.1:n.206A=
ENST00000684286.1:n.3614A=
ENST00000684502.1:n.3356A=
ENST00000684763.1:n.674A=
ENST00000366578.6:c.2059A= MANE Select ENSP00000355537.4:p.Asn687=
ENST00000492634.6:n.1989A=
ENST00000542672.6:c.2059A= ENSP00000443495.1:p.Asn687=
ENST00000651091.1:c.1749A= ENSP00000498677.1:n.1749A=
ENST00000651275.1:c.1951A= ENSP00000498926.1:p.Asn651=
ENST00000651781.1:c.1139A=
ENST00000651786.1:c.*1431A= ENSP00000498364.1:n.*1431A=
ENST00000652096.1:c.*1464A= ENSP00000498896.1:n.*1464A=
ENST00000366578.5:c.2059A= ENSP00000355537.4:p.Asn687=
ENST00000461367.1:n.268A=
ENST00000542672.5:c.2059A= ENSP00000443495.1:p.Asn687=
ENST00000546208.5:c.1435A= ENSP00000438384.2:p.Asn479=
NM_001103.3:c.2059A= NP_001094.1:p.Asn687=
NM_001278343.1:c.2059A= NP_001265272.1:p.Asn687=
NM_001278344.1:c.1435A= NP_001265273.1:p.Asn479=
NM_001278343.2:c.2059A= NP_001265272.1:p.Asn687=
NM_001103.4:c.2059A= MANE Select NP_001094.1:p.Asn687=
NM_001278344.2:c.1435A= NP_001265273.1:p.Asn479=