Canonical Allele Identifier: CA1430244734
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193643380C= , CM000665.2:g.193643380C= GRCh38
NC_000003.11:g.193361169C= , CM000665.1:g.193361169C= GRCh37
NC_000003.10:g.194843863C= NCBI36
NG_011605.1:g.55237C= , LRG_337:g.55237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361510.8:c.1313C= MANE Select ENSP00000355324.2:p.Ser438=
ENST00000361828.7:c.1148C= ENSP00000354429.3:p.Ser383=
ENST00000361908.8:c.1259C= ENSP00000354681.3:p.Ser420=
ENST00000392436.7:c.1148C= ENSP00000376231.3:p.Ser383=
ENST00000392437.6:c.1202C= ENSP00000376232.2:p.Ser401=
ENST00000642289.1:c.1087C=
ENST00000642445.1:c.1148C= ENSP00000495535.1:p.Ser383=
ENST00000642593.1:c.1148C= ENSP00000494273.1:p.Ser383=
ENST00000643329.1:c.830C= ENSP00000493673.1:p.Ser277=
ENST00000643737.1:c.*1229C= ENSP00000494210.1:n.*1229C=
ENST00000644595.1:c.1148C= ENSP00000494121.1:p.Ser383=
ENST00000644629.1:c.808C=
ENST00000644841.1:c.776C= ENSP00000493988.1:p.Ser259=
ENST00000644959.1:c.1117C=
ENST00000645553.1:c.1163C= ENSP00000494725.1:p.Ser388=
ENST00000646085.1:c.*626C= ENSP00000494509.1:n.*626C=
ENST00000646277.1:c.1313C= ENSP00000495289.1:p.Ser438=
ENST00000646544.1:c.136C=
ENST00000646699.1:c.1087C=
ENST00000646793.1:c.1040C= ENSP00000494512.1:p.Ser347=
ENST00000361150.6:c.1151C= ENSP00000354781.2:p.Ser384=
ENST00000361510.6:c.1313C= ENSP00000355324.2:p.Ser438=
ENST00000361715.6:c.1205C= ENSP00000355311.2:p.Ser402=
ENST00000361828.6:c.1202C= ENSP00000354429.2:p.Ser401=
ENST00000361908.7:c.1259C= ENSP00000354681.3:p.Ser420=
ENST00000392438.7:c.1148C= ENSP00000376233.3:p.Ser383=
ENST00000475899.1:n.344C=
NM_015560.2:c.1148C= , LRG_337t1:c.1148C= NP_056375.2:p.Ser383=
NM_130831.2:c.1040C= NP_570844.1:p.Ser347=
NM_130832.2:c.1094C= NP_570845.1:p.Ser365=
NM_130833.2:c.1151C= NP_570846.1:p.Ser384=
NM_130834.2:c.1202C= NP_570847.2:p.Ser401=
NM_130835.2:c.1205C= NP_570848.1:p.Ser402=
NM_130836.2:c.1259C= NP_570849.2:p.Ser420=
NM_130837.2:c.1313C= , LRG_337t2:c.1313C= NP_570850.2:p.Ser438=
XM_011512863.1:c.1313C= XP_011511165.1:p.Ser438=
XM_011512864.1:c.1259C= XP_011511166.1:p.Ser420=
XM_011512865.1:c.1202C= XP_011511167.1:p.Ser401=
XM_011512866.1:c.1151C= XP_011511168.1:p.Ser384=
XM_011512867.1:c.1148C= XP_011511169.1:p.Ser383=
XM_011512868.1:c.1040C= XP_011511170.1:p.Ser347=
XM_011512869.1:c.1313C= XP_011511171.1:p.Ser438=
NM_001354663.1:c.779C= NP_001341592.1:p.Ser260=
NM_001354664.1:c.776C= NP_001341593.1:p.Ser259=
XR_001740158.2:n.1542C=
XR_001740159.2:n.1377C=
NM_001354663.2:c.779C= NP_001341592.1:p.Ser260=
NM_001354664.2:c.776C= NP_001341593.1:p.Ser259=
NM_130831.3:c.1040C= NP_570844.1:p.Ser347=
NM_130832.3:c.1094C= NP_570845.1:p.Ser365=
NM_130834.3:c.1202C= NP_570847.2:p.Ser401=
NM_130836.3:c.1259C= NP_570849.2:p.Ser420=
NM_015560.3:c.1148C= NP_056375.2:p.Ser383=
NM_130833.3:c.1151C= NP_570846.1:p.Ser384=
NM_130835.3:c.1205C= NP_570848.1:p.Ser402=
NM_130837.3:c.1313C= MANE Select NP_570850.2:p.Ser438=