Canonical Allele Identifier: CA1430243545
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193642777G= , CM000665.2:g.193642777G= GRCh38
NC_000003.11:g.193360566G= , CM000665.1:g.193360566G= GRCh37
NC_000003.10:g.194843260G= NCBI36
NG_011605.1:g.54634G= , LRG_337:g.54634G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361510.8:c.1162G= MANE Select ENSP00000355324.2:p.Glu388=
ENST00000361828.7:c.997G= ENSP00000354429.3:p.Glu333=
ENST00000361908.8:c.1108G= ENSP00000354681.3:p.Glu370=
ENST00000392436.7:c.997G= ENSP00000376231.3:p.Glu333=
ENST00000392437.6:c.1051G= ENSP00000376232.2:p.Glu351=
ENST00000642289.1:c.1080-596G=
ENST00000642445.1:c.997G= ENSP00000495535.1:p.Glu333=
ENST00000642593.1:c.997G= ENSP00000494273.1:p.Glu333=
ENST00000643329.1:c.679G= ENSP00000493673.1:p.Glu227=
ENST00000643737.1:c.*1078G= ENSP00000494210.1:n.*1078G=
ENST00000644595.1:c.997G= ENSP00000494121.1:p.Glu333=
ENST00000644629.1:c.657G=
ENST00000644841.1:c.625G= ENSP00000493988.1:p.Glu209=
ENST00000644959.1:c.966G=
ENST00000645553.1:c.1012G= ENSP00000494725.1:p.Glu338=
ENST00000646085.1:c.*475G= ENSP00000494509.1:n.*475G=
ENST00000646277.1:c.1162G= ENSP00000495289.1:p.Glu388=
ENST00000646544.1:c.60G=
ENST00000646699.1:c.1080-596G=
ENST00000646793.1:c.889G= ENSP00000494512.1:p.Glu297=
ENST00000361150.6:c.1000G= ENSP00000354781.2:p.Glu334=
ENST00000361510.6:c.1162G= ENSP00000355324.2:p.Glu388=
ENST00000361715.6:c.1054G= ENSP00000355311.2:p.Glu352=
ENST00000361828.6:c.1051G= ENSP00000354429.2:p.Glu351=
ENST00000361908.7:c.1108G= ENSP00000354681.3:p.Glu370=
ENST00000392438.7:c.997G= ENSP00000376233.3:p.Glu333=
ENST00000475899.1:n.193G=
ENST00000497189.5:n.483G=
NM_015560.2:c.997G= , LRG_337t1:c.997G= NP_056375.2:p.Glu333=
NM_130831.2:c.889G= NP_570844.1:p.Glu297=
NM_130832.2:c.943G= NP_570845.1:p.Glu315=
NM_130833.2:c.1000G= NP_570846.1:p.Glu334=
NM_130834.2:c.1051G= NP_570847.2:p.Glu351=
NM_130835.2:c.1054G= NP_570848.1:p.Glu352=
NM_130836.2:c.1108G= NP_570849.2:p.Glu370=
NM_130837.2:c.1162G= , LRG_337t2:c.1162G= NP_570850.2:p.Glu388=
XM_011512863.1:c.1162G= XP_011511165.1:p.Glu388=
XM_011512864.1:c.1108G= XP_011511166.1:p.Glu370=
XM_011512865.1:c.1051G= XP_011511167.1:p.Glu351=
XM_011512866.1:c.1000G= XP_011511168.1:p.Glu334=
XM_011512867.1:c.997G= XP_011511169.1:p.Glu333=
XM_011512868.1:c.889G= XP_011511170.1:p.Glu297=
XM_011512869.1:c.1162G= XP_011511171.1:p.Glu388=
NM_001354663.1:c.628G= NP_001341592.1:p.Glu210=
NM_001354664.1:c.625G= NP_001341593.1:p.Glu209=
XR_001740158.2:n.1391G=
XR_001740159.2:n.1226G=
NM_001354663.2:c.628G= NP_001341592.1:p.Glu210=
NM_001354664.2:c.625G= NP_001341593.1:p.Glu209=
NM_130831.3:c.889G= NP_570844.1:p.Glu297=
NM_130832.3:c.943G= NP_570845.1:p.Glu315=
NM_130834.3:c.1051G= NP_570847.2:p.Glu351=
NM_130836.3:c.1108G= NP_570849.2:p.Glu370=
NM_015560.3:c.997G= NP_056375.2:p.Glu333=
NM_130833.3:c.1000G= NP_570846.1:p.Glu334=
NM_130835.3:c.1054G= NP_570848.1:p.Glu352=
NM_130837.3:c.1162G= MANE Select NP_570850.2:p.Glu388=