Canonical Allele Identifier: CA2487053205
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762530A= , CM000663.2:g.236762530A= GRCh38
NC_000001.10:g.236925830A= , CM000663.1:g.236925830A= GRCh37
NC_000001.9:g.234992453A= NCBI36
NG_009081.1:g.81061A=
NG_009081.2:g.103390A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2596A= ENSP00000443495.1:p.Met866=
ENST00000461367.2:n.892A=
ENST00000492634.7:n.2526A=
ENST00000682015.1:c.2503A= ENSP00000506961.1:p.Met835=
ENST00000682490.1:n.514A=
ENST00000682692.1:n.3691A=
ENST00000682966.1:n.8237A=
ENST00000683111.1:c.*1882A= ENSP00000507913.1:n.*1882A=
ENST00000683322.1:n.3948A=
ENST00000683805.1:n.1387A=
ENST00000684050.1:n.5234A=
ENST00000684122.1:n.2030A=
ENST00000684286.1:n.4151A=
ENST00000684502.1:n.3893A=
ENST00000684763.1:n.1211A=
ENST00000366578.6:c.2596A= MANE Select ENSP00000355537.4:p.Met866=
ENST00000492634.6:n.2526A=
ENST00000542672.6:c.2596A= ENSP00000443495.1:p.Met866=
ENST00000651091.1:c.2286A= ENSP00000498677.1:n.2286A=
ENST00000651275.1:c.2488A= ENSP00000498926.1:p.Met830=
ENST00000651781.1:c.1676A=
ENST00000651786.1:c.*1968A= ENSP00000498364.1:n.*1968A=
ENST00000652096.1:c.*2001A= ENSP00000498896.1:n.*2001A=
ENST00000366578.5:c.2596A= ENSP00000355537.4:p.Met866=
ENST00000461367.1:n.805A=
ENST00000542672.5:c.2596A= ENSP00000443495.1:p.Met866=
ENST00000546208.5:c.1972A= ENSP00000438384.2:p.Met658=
NM_001103.3:c.2596A= NP_001094.1:p.Met866=
NM_001278343.1:c.2596A= NP_001265272.1:p.Met866=
NM_001278344.1:c.1972A= NP_001265273.1:p.Met658=
NM_001278343.2:c.2596A= NP_001265272.1:p.Met866=
NM_001103.4:c.2596A= MANE Select NP_001094.1:p.Met866=
NM_001278344.2:c.1972A= NP_001265273.1:p.Met658=