Canonical Allele Identifier: CA2759937914
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193643250_193643251insAGA , CM000665.2:g.193643250_193643251insAGA GRCh38
NC_000003.11:g.193361039_193361040insAGA , CM000665.1:g.193361039_193361040insAGA GRCh37
NC_000003.10:g.194843733_194843734insAGA NCBI36
NG_011605.1:g.55107_55108insAGA , LRG_337:g.55107_55108insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361510.8:c.1306-123_1306-122insAGA MANE Select ENSP00000355324.2:n.1306-123_1306-122insAGA
ENST00000361828.7:c.1141-123_1141-122insAGA ENSP00000354429.3:n.1141-123_1141-122insAGA
ENST00000361908.8:c.1252-123_1252-122insAGA ENSP00000354681.3:n.1252-123_1252-122insAGA
ENST00000392436.7:c.1141-123_1141-122insAGA ENSP00000376231.3:n.1141-123_1141-122insAGA
ENST00000392437.6:c.1195-123_1195-122insAGA ENSP00000376232.2:n.1195-123_1195-122insAGA
ENST00000642289.1:c.1080-123_1080-122insAGA
ENST00000642445.1:c.1141-123_1141-122insAGA ENSP00000495535.1:n.1141-123_1141-122insAGA
ENST00000642593.1:c.1141-123_1141-122insAGA ENSP00000494273.1:n.1141-123_1141-122insAGA
ENST00000643329.1:c.823-123_823-122insAGA ENSP00000493673.1:n.823-123_823-122insAGA
ENST00000643737.1:c.*1222-123_*1222-122insAGA ENSP00000494210.1:n.*1222-123_*1222-122insAGA
ENST00000644595.1:c.1141-123_1141-122insAGA ENSP00000494121.1:n.1141-123_1141-122insAGA
ENST00000644629.1:c.801-123_801-122insAGA
ENST00000644841.1:c.769-123_769-122insAGA ENSP00000493988.1:n.769-123_769-122insAGA
ENST00000644959.1:c.1110-123_1110-122insAGA
ENST00000645553.1:c.1156-123_1156-122insAGA ENSP00000494725.1:n.1156-123_1156-122insAGA
ENST00000646085.1:c.*619-123_*619-122insAGA ENSP00000494509.1:n.*619-123_*619-122insAGA
ENST00000646277.1:c.1306-123_1306-122insAGA ENSP00000495289.1:n.1306-123_1306-122insAGA
ENST00000646544.1:c.129-123_129-122insAGA
ENST00000646699.1:c.1080-123_1080-122insAGA
ENST00000646793.1:c.1033-123_1033-122insAGA ENSP00000494512.1:n.1033-123_1033-122insAGA
ENST00000361150.6:c.1144-123_1144-122insAGA ENSP00000354781.2:n.1144-123_1144-122insAGA
ENST00000361510.6:c.1306-123_1306-122insAGA ENSP00000355324.2:n.1306-123_1306-122insAGA
ENST00000361715.6:c.1198-123_1198-122insAGA ENSP00000355311.2:n.1198-123_1198-122insAGA
ENST00000361828.6:c.1195-123_1195-122insAGA ENSP00000354429.2:n.1195-123_1195-122insAGA
ENST00000361908.7:c.1252-123_1252-122insAGA ENSP00000354681.3:n.1252-123_1252-122insAGA
ENST00000392438.7:c.1141-123_1141-122insAGA ENSP00000376233.3:n.1141-123_1141-122insAGA
ENST00000475899.1:n.337-123_337-122insAGA
NM_015560.2:c.1141-123_1141-122insAGA , LRG_337t1:c.1141-123_1141-122insAGA NP_056375.2:n.1141-123_1141-122insAGA
NM_130831.2:c.1033-123_1033-122insAGA NP_570844.1:n.1033-123_1033-122insAGA
NM_130832.2:c.1087-123_1087-122insAGA NP_570845.1:n.1087-123_1087-122insAGA
NM_130833.2:c.1144-123_1144-122insAGA NP_570846.1:n.1144-123_1144-122insAGA
NM_130834.2:c.1195-123_1195-122insAGA NP_570847.2:n.1195-123_1195-122insAGA
NM_130835.2:c.1198-123_1198-122insAGA NP_570848.1:n.1198-123_1198-122insAGA
NM_130836.2:c.1252-123_1252-122insAGA NP_570849.2:n.1252-123_1252-122insAGA
NM_130837.2:c.1306-123_1306-122insAGA , LRG_337t2:c.1306-123_1306-122insAGA NP_570850.2:n.1306-123_1306-122insAGA
XM_011512863.1:c.1306-123_1306-122insAGA XP_011511165.1:n.1306-123_1306-122insAGA
XM_011512864.1:c.1252-123_1252-122insAGA XP_011511166.1:n.1252-123_1252-122insAGA
XM_011512865.1:c.1195-123_1195-122insAGA XP_011511167.1:n.1195-123_1195-122insAGA
XM_011512866.1:c.1144-123_1144-122insAGA XP_011511168.1:n.1144-123_1144-122insAGA
XM_011512867.1:c.1141-123_1141-122insAGA XP_011511169.1:n.1141-123_1141-122insAGA
XM_011512868.1:c.1033-123_1033-122insAGA XP_011511170.1:n.1033-123_1033-122insAGA
XM_011512869.1:c.1306-123_1306-122insAGA XP_011511171.1:n.1306-123_1306-122insAGA
NM_001354663.1:c.772-123_772-122insAGA NP_001341592.1:n.772-123_772-122insAGA
NM_001354664.1:c.769-123_769-122insAGA NP_001341593.1:n.769-123_769-122insAGA
XR_001740158.2:n.1535-123_1535-122insAGA
XR_001740159.2:n.1370-123_1370-122insAGA
NM_001354663.2:c.772-123_772-122insAGA NP_001341592.1:n.772-123_772-122insAGA
NM_001354664.2:c.769-123_769-122insAGA NP_001341593.1:n.769-123_769-122insAGA
NM_130831.3:c.1033-123_1033-122insAGA NP_570844.1:n.1033-123_1033-122insAGA
NM_130832.3:c.1087-123_1087-122insAGA NP_570845.1:n.1087-123_1087-122insAGA
NM_130834.3:c.1195-123_1195-122insAGA NP_570847.2:n.1195-123_1195-122insAGA
NM_130836.3:c.1252-123_1252-122insAGA NP_570849.2:n.1252-123_1252-122insAGA
NM_015560.3:c.1141-123_1141-122insAGA NP_056375.2:n.1141-123_1141-122insAGA
NM_130833.3:c.1144-123_1144-122insAGA NP_570846.1:n.1144-123_1144-122insAGA
NM_130835.3:c.1198-123_1198-122insAGA NP_570848.1:n.1198-123_1198-122insAGA
NM_130837.3:c.1306-123_1306-122insAGA MANE Select NP_570850.2:n.1306-123_1306-122insAGA