Canonical Allele Identifier: CA1430245927

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193644014_193644015delinsTG , CM000665.2:g.193644014_193644015delinsTG	GRCh38
NC_000003.11:g.193361803_193361804delinsTG , CM000665.1:g.193361803_193361804delinsTG	GRCh37
NC_000003.10:g.194844497_194844498delinsTG	NCBI36
NG_011605.1:g.55871_55872delinsTG , LRG_337:g.55871_55872delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1517_1518delinsTG MANE Select	ENSP00000355324.2:p.Leu506=
ENST00000361828.7:c.1352_1353delinsTG	ENSP00000354429.3:p.Leu451=
ENST00000361908.8:c.1463_1464delinsTG	ENSP00000354681.3:p.Leu488=
ENST00000392436.7:c.1352_1353delinsTG	ENSP00000376231.3:p.Leu451=
ENST00000392437.6:c.1406_1407delinsTG	ENSP00000376232.2:p.Leu469=
ENST00000642289.1:c.1291_1292delinsTG
ENST00000642445.1:c.1352_1353delinsTG	ENSP00000495535.1:p.Leu451=
ENST00000642593.1:c.1352_1353delinsTG	ENSP00000494273.1:p.Leu451=
ENST00000643329.1:c.1034_1035delinsTG	ENSP00000493673.1:p.Leu345=
ENST00000643737.1:c.*1433_*1434delinsTG	ENSP00000494210.1:n.*1433_*1434delinsTG
ENST00000644595.1:c.1352_1353delinsTG	ENSP00000494121.1:p.Leu451=
ENST00000644629.1:c.1012_1013delinsTG
ENST00000644841.1:c.980_981delinsTG	ENSP00000493988.1:p.Leu327=
ENST00000644959.1:c.1321_1322delinsTG
ENST00000645553.1:c.1367_1368delinsTG	ENSP00000494725.1:p.Leu456=
ENST00000646085.1:c.*830_*831delinsTG	ENSP00000494509.1:n.*830_*831delinsTG
ENST00000646277.1:c.1540_1541delinsTG	ENSP00000495289.1:p.Trp514=
ENST00000646544.1:c.340_341delinsTG
ENST00000646699.1:c.1291_1292delinsTG
ENST00000646793.1:c.1244_1245delinsTG	ENSP00000494512.1:p.Leu415=
ENST00000361150.6:c.1355_1356delinsTG	ENSP00000354781.2:p.Leu452=
ENST00000361510.6:c.1517_1518delinsTG	ENSP00000355324.2:p.Leu506=
ENST00000361715.6:c.1409_1410delinsTG	ENSP00000355311.2:p.Leu470=
ENST00000361828.6:c.1406_1407delinsTG	ENSP00000354429.2:p.Leu469=
ENST00000361908.7:c.1463_1464delinsTG	ENSP00000354681.3:p.Leu488=
ENST00000392438.7:c.1352_1353delinsTG	ENSP00000376233.3:p.Leu451=
ENST00000475899.1:n.548_549delinsTG
NM_015560.2:c.1352_1353delinsTG , LRG_337t1:c.1352_1353delinsTG	NP_056375.2:p.Leu451=
NM_130831.2:c.1244_1245delinsTG	NP_570844.1:p.Leu415=
NM_130832.2:c.1298_1299delinsTG	NP_570845.1:p.Leu433=
NM_130833.2:c.1355_1356delinsTG	NP_570846.1:p.Leu452=
NM_130834.2:c.1406_1407delinsTG	NP_570847.2:p.Leu469=
NM_130835.2:c.1409_1410delinsTG	NP_570848.1:p.Leu470=
NM_130836.2:c.1463_1464delinsTG	NP_570849.2:p.Leu488=
NM_130837.2:c.1517_1518delinsTG , LRG_337t2:c.1517_1518delinsTG	NP_570850.2:p.Leu506=
XM_011512863.1:c.1517_1518delinsTG	XP_011511165.1:p.Leu506=
XM_011512864.1:c.1463_1464delinsTG	XP_011511166.1:p.Leu488=
XM_011512865.1:c.1406_1407delinsTG	XP_011511167.1:p.Leu469=
XM_011512866.1:c.1355_1356delinsTG	XP_011511168.1:p.Leu452=
XM_011512867.1:c.1352_1353delinsTG	XP_011511169.1:p.Leu451=
XM_011512868.1:c.1244_1245delinsTG	XP_011511170.1:p.Leu415=
XM_011512869.1:c.1517_1518delinsTG	XP_011511171.1:p.Leu506=
NM_001354663.1:c.983_984delinsTG	NP_001341592.1:p.Leu328=
NM_001354664.1:c.980_981delinsTG	NP_001341593.1:p.Leu327=
XR_001740158.2:n.1746_1747delinsTG
XR_001740159.2:n.1581_1582delinsTG
NM_001354663.2:c.983_984delinsTG	NP_001341592.1:p.Leu328=
NM_001354664.2:c.980_981delinsTG	NP_001341593.1:p.Leu327=
NM_130831.3:c.1244_1245delinsTG	NP_570844.1:p.Leu415=
NM_130832.3:c.1298_1299delinsTG	NP_570845.1:p.Leu433=
NM_130834.3:c.1406_1407delinsTG	NP_570847.2:p.Leu469=
NM_130836.3:c.1463_1464delinsTG	NP_570849.2:p.Leu488=
NM_015560.3:c.1352_1353delinsTG	NP_056375.2:p.Leu451=
NM_130833.3:c.1355_1356delinsTG	NP_570846.1:p.Leu452=
NM_130835.3:c.1409_1410delinsTG	NP_570848.1:p.Leu470=
NM_130837.3:c.1517_1518delinsTG MANE Select	NP_570850.2:p.Leu506=