Canonical Allele Identifier: CA2669102913
Gene: OPA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193637902_193637907del , CM000665.2:g.193637902_193637907del GRCh38
NC_000003.11:g.193355691_193355696del , CM000665.1:g.193355691_193355696del GRCh37
NC_000003.10:g.194838385_194838390del NCBI36
NG_011605.1:g.49759_49764del , LRG_337:g.49759_49764del

Transcript Alleles

HGVS Amino-acid change
ENST00000361510.8:c.1036-50_1036-45del MANE Select ENSP00000355324.2:n.1036-50_1036-45del
ENST00000361828.7:c.871-50_871-45del ENSP00000354429.3:n.871-50_871-45del
ENST00000361908.8:c.982-50_982-45del ENSP00000354681.3:n.982-50_982-45del
ENST00000392436.7:c.871-50_871-45del ENSP00000376231.3:n.871-50_871-45del
ENST00000392437.6:c.925-50_925-45del ENSP00000376232.2:n.925-50_925-45del
ENST00000642289.1:c.966-50_966-45del
ENST00000642445.1:c.871-50_871-45del ENSP00000495535.1:n.871-50_871-45del
ENST00000642593.1:c.871-50_871-45del ENSP00000494273.1:n.871-50_871-45del
ENST00000643329.1:c.553-50_553-45del ENSP00000493673.1:n.553-50_553-45del
ENST00000643737.1:c.*952-50_*952-45del ENSP00000494210.1:n.*952-50_*952-45del
ENST00000644595.1:c.871-50_871-45del ENSP00000494121.1:n.871-50_871-45del
ENST00000644629.1:c.531-50_531-45del
ENST00000644841.1:c.499-50_499-45del ENSP00000493988.1:n.499-50_499-45del
ENST00000644959.1:c.840-50_840-45del
ENST00000645553.1:c.886-50_886-45del ENSP00000494725.1:n.886-50_886-45del
ENST00000646085.1:c.*349-50_*349-45del ENSP00000494509.1:n.*349-50_*349-45del
ENST00000646277.1:c.1036-50_1036-45del ENSP00000495289.1:n.1036-50_1036-45del
ENST00000646699.1:c.966-50_966-45del
ENST00000646793.1:c.763-50_763-45del ENSP00000494512.1:n.763-50_763-45del
ENST00000361150.6:c.874-50_874-45del ENSP00000354781.2:n.874-50_874-45del
ENST00000361510.6:c.1036-50_1036-45del ENSP00000355324.2:n.1036-50_1036-45del
ENST00000361715.6:c.928-50_928-45del ENSP00000355311.2:n.928-50_928-45del
ENST00000361828.6:c.925-50_925-45del ENSP00000354429.2:n.925-50_925-45del
ENST00000361908.7:c.982-50_982-45del ENSP00000354681.3:n.982-50_982-45del
ENST00000392438.7:c.871-50_871-45del ENSP00000376233.3:n.871-50_871-45del
ENST00000475899.1:n.67-50_67-45del
ENST00000495476.1:n.392-50_392-45del
ENST00000497189.5:n.357-50_357-45del
NM_015560.2:c.871-50_871-45del , LRG_337t1:c.871-50_871-45del NP_056375.2:n.871-50_871-45del
NM_130831.2:c.763-50_763-45del NP_570844.1:n.763-50_763-45del
NM_130832.2:c.817-50_817-45del NP_570845.1:n.817-50_817-45del
NM_130833.2:c.874-50_874-45del NP_570846.1:n.874-50_874-45del
NM_130834.2:c.925-50_925-45del NP_570847.2:n.925-50_925-45del
NM_130835.2:c.928-50_928-45del NP_570848.1:n.928-50_928-45del
NM_130836.2:c.982-50_982-45del NP_570849.2:n.982-50_982-45del
NM_130837.2:c.1036-50_1036-45del , LRG_337t2:c.1036-50_1036-45del NP_570850.2:n.1036-50_1036-45del
XM_011512863.1:c.1036-50_1036-45del XP_011511165.1:n.1036-50_1036-45del
XM_011512864.1:c.982-50_982-45del XP_011511166.1:n.982-50_982-45del
XM_011512865.1:c.925-50_925-45del XP_011511167.1:n.925-50_925-45del
XM_011512866.1:c.874-50_874-45del XP_011511168.1:n.874-50_874-45del
XM_011512867.1:c.871-50_871-45del XP_011511169.1:n.871-50_871-45del
XM_011512868.1:c.763-50_763-45del XP_011511170.1:n.763-50_763-45del
XM_011512869.1:c.1036-50_1036-45del XP_011511171.1:n.1036-50_1036-45del
NM_001354663.1:c.502-50_502-45del NP_001341592.1:n.502-50_502-45del
NM_001354664.1:c.499-50_499-45del NP_001341593.1:n.499-50_499-45del
XR_001740158.2:n.1265-50_1265-45del
XR_001740159.2:n.1100-50_1100-45del
NM_001354663.2:c.502-50_502-45del NP_001341592.1:n.502-50_502-45del
NM_001354664.2:c.499-50_499-45del NP_001341593.1:n.499-50_499-45del
NM_130831.3:c.763-50_763-45del NP_570844.1:n.763-50_763-45del
NM_130832.3:c.817-50_817-45del NP_570845.1:n.817-50_817-45del
NM_130834.3:c.925-50_925-45del NP_570847.2:n.925-50_925-45del
NM_130836.3:c.982-50_982-45del NP_570849.2:n.982-50_982-45del
NM_015560.3:c.871-50_871-45del NP_056375.2:n.871-50_871-45del
NM_130833.3:c.874-50_874-45del NP_570846.1:n.874-50_874-45del
NM_130835.3:c.928-50_928-45del NP_570848.1:n.928-50_928-45del
NM_130837.3:c.1036-50_1036-45del MANE Select NP_570850.2:n.1036-50_1036-45del