Canonical Allele Identifier: CA1430250459
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193647044_193647045delinsCT , CM000665.2:g.193647044_193647045delinsCT GRCh38
NC_000003.11:g.193364833_193364834delinsCT , CM000665.1:g.193364833_193364834delinsCT GRCh37
NC_000003.10:g.194847527_194847528delinsCT NCBI36
NG_011605.1:g.58901_58902delinsCT , LRG_337:g.58901_58902delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000361510.8:c.1755-21_1755-20delinsCT MANE Select ENSP00000355324.2:n.1755-21_1755-20delins...
ENST00000361828.7:c.1590-21_1590-20delinsCT ENSP00000354429.3:n.1590-21_1590-20delins...
ENST00000361908.8:c.1701-21_1701-20delinsCT ENSP00000354681.3:n.1701-21_1701-20delins...
ENST00000392436.7:c.1590-21_1590-20delinsCT ENSP00000376231.3:n.1590-21_1590-20delins...
ENST00000392437.6:c.1644-21_1644-20delinsCT ENSP00000376232.2:n.1644-21_1644-20delins...
ENST00000642289.1:c.1529-21_1529-20delinsCT
ENST00000642445.1:c.1590-21_1590-20delinsCT ENSP00000495535.1:n.1590-21_1590-20delins...
ENST00000642593.1:c.1590-21_1590-20delinsCT ENSP00000494273.1:n.1590-21_1590-20delins...
ENST00000643329.1:c.1272-21_1272-20delinsCT ENSP00000493673.1:n.1272-21_1272-20delins...
ENST00000643737.1:c.*1671-21_*1671-20delinsCT ENSP00000494210.1:n.*1671-21_*1671-20deli...
ENST00000644595.1:c.1590-21_1590-20delinsCT ENSP00000494121.1:n.1590-21_1590-20delins...
ENST00000644629.1:c.1177-21_1177-20delinsCT
ENST00000644841.1:c.*74-21_*74-20delinsCT ENSP00000493988.1:n.*74-21_*74-20delinsCT...
ENST00000644959.1:c.1559-21_1559-20delinsCT
ENST00000645553.1:c.1605-21_1605-20delinsCT ENSP00000494725.1:n.1605-21_1605-20delins...
ENST00000646085.1:c.*1068-21_*1068-20delinsCT ENSP00000494509.1:n.*1068-21_*1068-20deli...
ENST00000646277.1:c.*191-21_*191-20delinsCT ENSP00000495289.1:n.*191-21_*191-20delins...
ENST00000646544.1:c.578-21_578-20delinsCT
ENST00000646699.1:c.1529-21_1529-20delinsCT
ENST00000646793.1:c.1482-21_1482-20delinsCT ENSP00000494512.1:n.1482-21_1482-20delins...
ENST00000361150.6:c.1593-21_1593-20delinsCT ENSP00000354781.2:n.1593-21_1593-20delins...
ENST00000361510.6:c.1755-21_1755-20delinsCT ENSP00000355324.2:n.1755-21_1755-20delins...
ENST00000361715.6:c.1647-21_1647-20delinsCT ENSP00000355311.2:n.1647-21_1647-20delins...
ENST00000361828.6:c.1644-21_1644-20delinsCT ENSP00000354429.2:n.1644-21_1644-20delins...
ENST00000361908.7:c.1701-21_1701-20delinsCT ENSP00000354681.3:n.1701-21_1701-20delins...
ENST00000392438.7:c.1590-21_1590-20delinsCT ENSP00000376233.3:n.1590-21_1590-20delins...
ENST00000483516.1:n.88-21_88-20delinsCT
NM_015560.2:c.1590-21_1590-20delinsCT , LRG_337t1:c.1590-21_1590-20delinsCT NP_056375.2:n.1590-21_1590-20delinsCT
NM_130831.2:c.1482-21_1482-20delinsCT NP_570844.1:n.1482-21_1482-20delinsCT
NM_130832.2:c.1536-21_1536-20delinsCT NP_570845.1:n.1536-21_1536-20delinsCT
NM_130833.2:c.1593-21_1593-20delinsCT NP_570846.1:n.1593-21_1593-20delinsCT
NM_130834.2:c.1644-21_1644-20delinsCT NP_570847.2:n.1644-21_1644-20delinsCT
NM_130835.2:c.1647-21_1647-20delinsCT NP_570848.1:n.1647-21_1647-20delinsCT
NM_130836.2:c.1701-21_1701-20delinsCT NP_570849.2:n.1701-21_1701-20delinsCT
NM_130837.2:c.1755-21_1755-20delinsCT , LRG_337t2:c.1755-21_1755-20delinsCT NP_570850.2:n.1755-21_1755-20delinsCT
XM_011512863.1:c.1755-21_1755-20delinsCT XP_011511165.1:n.1755-21_1755-20delinsCT
XM_011512864.1:c.1701-21_1701-20delinsCT XP_011511166.1:n.1701-21_1701-20delinsCT
XM_011512865.1:c.1644-21_1644-20delinsCT XP_011511167.1:n.1644-21_1644-20delinsCT
XM_011512866.1:c.1593-21_1593-20delinsCT XP_011511168.1:n.1593-21_1593-20delinsCT
XM_011512867.1:c.1590-21_1590-20delinsCT XP_011511169.1:n.1590-21_1590-20delinsCT
XM_011512868.1:c.1482-21_1482-20delinsCT XP_011511170.1:n.1482-21_1482-20delinsCT
XM_011512869.1:c.1755-21_1755-20delinsCT XP_011511171.1:n.1755-21_1755-20delinsCT
NM_001354663.1:c.1221-21_1221-20delinsCT NP_001341592.1:n.1221-21_1221-20delinsCT
NM_001354664.1:c.1218-21_1218-20delinsCT NP_001341593.1:n.1218-21_1218-20delinsCT
XR_001740158.2:n.1984-21_1984-20delinsCT
XR_001740159.2:n.1819-21_1819-20delinsCT
NM_001354663.2:c.1221-21_1221-20delinsCT NP_001341592.1:n.1221-21_1221-20delinsCT
NM_001354664.2:c.1218-21_1218-20delinsCT NP_001341593.1:n.1218-21_1218-20delinsCT
NM_130831.3:c.1482-21_1482-20delinsCT NP_570844.1:n.1482-21_1482-20delinsCT
NM_130832.3:c.1536-21_1536-20delinsCT NP_570845.1:n.1536-21_1536-20delinsCT
NM_130834.3:c.1644-21_1644-20delinsCT NP_570847.2:n.1644-21_1644-20delinsCT
NM_130836.3:c.1701-21_1701-20delinsCT NP_570849.2:n.1701-21_1701-20delinsCT
NM_015560.3:c.1590-21_1590-20delinsCT NP_056375.2:n.1590-21_1590-20delinsCT
NM_130833.3:c.1593-21_1593-20delinsCT NP_570846.1:n.1593-21_1593-20delinsCT
NM_130835.3:c.1647-21_1647-20delinsCT NP_570848.1:n.1647-21_1647-20delinsCT
NM_130837.3:c.1755-21_1755-20delinsCT MANE Select NP_570850.2:n.1755-21_1755-20delinsCT