Canonical Allele Identifier: CA2759937880

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643188_193643189insAGT , CM000665.2:g.193643188_193643189insAGT	GRCh38
NC_000003.11:g.193360977_193360978insAGT , CM000665.1:g.193360977_193360978insAGT	GRCh37
NC_000003.10:g.194843671_194843672insAGT	NCBI36
NG_011605.1:g.55045_55046insAGT , LRG_337:g.55045_55046insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1305+139_1305+140insAGT MANE Select	ENSP00000355324.2:n.1305+139_1305+140insAGT
ENST00000361828.7:c.1140+139_1140+140insAGT	ENSP00000354429.3:n.1140+139_1140+140insAGT
ENST00000361908.8:c.1251+139_1251+140insAGT	ENSP00000354681.3:n.1251+139_1251+140insAGT
ENST00000392436.7:c.1140+139_1140+140insAGT	ENSP00000376231.3:n.1140+139_1140+140insAGT
ENST00000392437.6:c.1194+139_1194+140insAGT	ENSP00000376232.2:n.1194+139_1194+140insAGT
ENST00000642289.1:c.1080-185_1080-184insAGT
ENST00000642445.1:c.1140+139_1140+140insAGT	ENSP00000495535.1:n.1140+139_1140+140insAGT
ENST00000642593.1:c.1140+139_1140+140insAGT	ENSP00000494273.1:n.1140+139_1140+140insAGT
ENST00000643329.1:c.822+139_822+140insAGT	ENSP00000493673.1:n.822+139_822+140insAGT
ENST00000643737.1:c.*1221+139_*1221+140insAGT	ENSP00000494210.1:n.*1221+139_*1221+140insAGT
ENST00000644595.1:c.1140+139_1140+140insAGT	ENSP00000494121.1:n.1140+139_1140+140insAGT
ENST00000644629.1:c.800+139_800+140insAGT
ENST00000644841.1:c.768+139_768+140insAGT	ENSP00000493988.1:n.768+139_768+140insAGT
ENST00000644959.1:c.1109+139_1109+140insAGT
ENST00000645553.1:c.1155+139_1155+140insAGT	ENSP00000494725.1:n.1155+139_1155+140insAGT
ENST00000646085.1:c.*618+139_*618+140insAGT	ENSP00000494509.1:n.*618+139_*618+140insAGT
ENST00000646277.1:c.1305+139_1305+140insAGT	ENSP00000495289.1:n.1305+139_1305+140insAGT
ENST00000646544.1:c.129-185_129-184insAGT
ENST00000646699.1:c.1080-185_1080-184insAGT
ENST00000646793.1:c.1032+139_1032+140insAGT	ENSP00000494512.1:n.1032+139_1032+140insAGT
ENST00000361150.6:c.1143+139_1143+140insAGT	ENSP00000354781.2:n.1143+139_1143+140insAGT
ENST00000361510.6:c.1305+139_1305+140insAGT	ENSP00000355324.2:n.1305+139_1305+140insAGT
ENST00000361715.6:c.1197+139_1197+140insAGT	ENSP00000355311.2:n.1197+139_1197+140insAGT
ENST00000361828.6:c.1194+139_1194+140insAGT	ENSP00000354429.2:n.1194+139_1194+140insAGT
ENST00000361908.7:c.1251+139_1251+140insAGT	ENSP00000354681.3:n.1251+139_1251+140insAGT
ENST00000392438.7:c.1140+139_1140+140insAGT	ENSP00000376233.3:n.1140+139_1140+140insAGT
ENST00000475899.1:n.336+139_336+140insAGT
NM_015560.2:c.1140+139_1140+140insAGT , LRG_337t1:c.1140+139_1140+140insAGT	NP_056375.2:n.1140+139_1140+140insAGT
NM_130831.2:c.1032+139_1032+140insAGT	NP_570844.1:n.1032+139_1032+140insAGT
NM_130832.2:c.1086+139_1086+140insAGT	NP_570845.1:n.1086+139_1086+140insAGT
NM_130833.2:c.1143+139_1143+140insAGT	NP_570846.1:n.1143+139_1143+140insAGT
NM_130834.2:c.1194+139_1194+140insAGT	NP_570847.2:n.1194+139_1194+140insAGT
NM_130835.2:c.1197+139_1197+140insAGT	NP_570848.1:n.1197+139_1197+140insAGT
NM_130836.2:c.1251+139_1251+140insAGT	NP_570849.2:n.1251+139_1251+140insAGT
NM_130837.2:c.1305+139_1305+140insAGT , LRG_337t2:c.1305+139_1305+140insAGT	NP_570850.2:n.1305+139_1305+140insAGT
XM_011512863.1:c.1305+139_1305+140insAGT	XP_011511165.1:n.1305+139_1305+140insAGT
XM_011512864.1:c.1251+139_1251+140insAGT	XP_011511166.1:n.1251+139_1251+140insAGT
XM_011512865.1:c.1194+139_1194+140insAGT	XP_011511167.1:n.1194+139_1194+140insAGT
XM_011512866.1:c.1143+139_1143+140insAGT	XP_011511168.1:n.1143+139_1143+140insAGT
XM_011512867.1:c.1140+139_1140+140insAGT	XP_011511169.1:n.1140+139_1140+140insAGT
XM_011512868.1:c.1032+139_1032+140insAGT	XP_011511170.1:n.1032+139_1032+140insAGT
XM_011512869.1:c.1305+139_1305+140insAGT	XP_011511171.1:n.1305+139_1305+140insAGT
NM_001354663.1:c.771+139_771+140insAGT	NP_001341592.1:n.771+139_771+140insAGT
NM_001354664.1:c.768+139_768+140insAGT	NP_001341593.1:n.768+139_768+140insAGT
XR_001740158.2:n.1534+139_1534+140insAGT
XR_001740159.2:n.1369+139_1369+140insAGT
NM_001354663.2:c.771+139_771+140insAGT	NP_001341592.1:n.771+139_771+140insAGT
NM_001354664.2:c.768+139_768+140insAGT	NP_001341593.1:n.768+139_768+140insAGT
NM_130831.3:c.1032+139_1032+140insAGT	NP_570844.1:n.1032+139_1032+140insAGT
NM_130832.3:c.1086+139_1086+140insAGT	NP_570845.1:n.1086+139_1086+140insAGT
NM_130834.3:c.1194+139_1194+140insAGT	NP_570847.2:n.1194+139_1194+140insAGT
NM_130836.3:c.1251+139_1251+140insAGT	NP_570849.2:n.1251+139_1251+140insAGT
NM_015560.3:c.1140+139_1140+140insAGT	NP_056375.2:n.1140+139_1140+140insAGT
NM_130833.3:c.1143+139_1143+140insAGT	NP_570846.1:n.1143+139_1143+140insAGT
NM_130835.3:c.1197+139_1197+140insAGT	NP_570848.1:n.1197+139_1197+140insAGT
NM_130837.3:c.1305+139_1305+140insAGT MANE Select	NP_570850.2:n.1305+139_1305+140insAGT