Canonical Allele Identifier: CA2759937900

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643206_193643207insACA , CM000665.2:g.193643206_193643207insACA	GRCh38
NC_000003.11:g.193360995_193360996insACA , CM000665.1:g.193360995_193360996insACA	GRCh37
NC_000003.10:g.194843689_194843690insACA	NCBI36
NG_011605.1:g.55063_55064insACA , LRG_337:g.55063_55064insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1305+157_1305+158insACA MANE Select	ENSP00000355324.2:n.1305+157_1305+158insACA
ENST00000361828.7:c.1140+157_1140+158insACA	ENSP00000354429.3:n.1140+157_1140+158insACA
ENST00000361908.8:c.1251+157_1251+158insACA	ENSP00000354681.3:n.1251+157_1251+158insACA
ENST00000392436.7:c.1140+157_1140+158insACA	ENSP00000376231.3:n.1140+157_1140+158insACA
ENST00000392437.6:c.1194+157_1194+158insACA	ENSP00000376232.2:n.1194+157_1194+158insACA
ENST00000642289.1:c.1080-167_1080-166insACA
ENST00000642445.1:c.1140+157_1140+158insACA	ENSP00000495535.1:n.1140+157_1140+158insACA
ENST00000642593.1:c.1140+157_1140+158insACA	ENSP00000494273.1:n.1140+157_1140+158insACA
ENST00000643329.1:c.822+157_822+158insACA	ENSP00000493673.1:n.822+157_822+158insACA
ENST00000643737.1:c.*1221+157_*1221+158insACA	ENSP00000494210.1:n.*1221+157_*1221+158insACA
ENST00000644595.1:c.1140+157_1140+158insACA	ENSP00000494121.1:n.1140+157_1140+158insACA
ENST00000644629.1:c.800+157_800+158insACA
ENST00000644841.1:c.768+157_768+158insACA	ENSP00000493988.1:n.768+157_768+158insACA
ENST00000644959.1:c.1109+157_1109+158insACA
ENST00000645553.1:c.1155+157_1155+158insACA	ENSP00000494725.1:n.1155+157_1155+158insACA
ENST00000646085.1:c.*618+157_*618+158insACA	ENSP00000494509.1:n.*618+157_*618+158insACA
ENST00000646277.1:c.1305+157_1305+158insACA	ENSP00000495289.1:n.1305+157_1305+158insACA
ENST00000646544.1:c.129-167_129-166insACA
ENST00000646699.1:c.1080-167_1080-166insACA
ENST00000646793.1:c.1032+157_1032+158insACA	ENSP00000494512.1:n.1032+157_1032+158insACA
ENST00000361150.6:c.1143+157_1143+158insACA	ENSP00000354781.2:n.1143+157_1143+158insACA
ENST00000361510.6:c.1305+157_1305+158insACA	ENSP00000355324.2:n.1305+157_1305+158insACA
ENST00000361715.6:c.1197+157_1197+158insACA	ENSP00000355311.2:n.1197+157_1197+158insACA
ENST00000361828.6:c.1194+157_1194+158insACA	ENSP00000354429.2:n.1194+157_1194+158insACA
ENST00000361908.7:c.1251+157_1251+158insACA	ENSP00000354681.3:n.1251+157_1251+158insACA
ENST00000392438.7:c.1140+157_1140+158insACA	ENSP00000376233.3:n.1140+157_1140+158insACA
ENST00000475899.1:n.336+157_336+158insACA
NM_015560.2:c.1140+157_1140+158insACA , LRG_337t1:c.1140+157_1140+158insACA	NP_056375.2:n.1140+157_1140+158insACA
NM_130831.2:c.1032+157_1032+158insACA	NP_570844.1:n.1032+157_1032+158insACA
NM_130832.2:c.1086+157_1086+158insACA	NP_570845.1:n.1086+157_1086+158insACA
NM_130833.2:c.1143+157_1143+158insACA	NP_570846.1:n.1143+157_1143+158insACA
NM_130834.2:c.1194+157_1194+158insACA	NP_570847.2:n.1194+157_1194+158insACA
NM_130835.2:c.1197+157_1197+158insACA	NP_570848.1:n.1197+157_1197+158insACA
NM_130836.2:c.1251+157_1251+158insACA	NP_570849.2:n.1251+157_1251+158insACA
NM_130837.2:c.1305+157_1305+158insACA , LRG_337t2:c.1305+157_1305+158insACA	NP_570850.2:n.1305+157_1305+158insACA
XM_011512863.1:c.1305+157_1305+158insACA	XP_011511165.1:n.1305+157_1305+158insACA
XM_011512864.1:c.1251+157_1251+158insACA	XP_011511166.1:n.1251+157_1251+158insACA
XM_011512865.1:c.1194+157_1194+158insACA	XP_011511167.1:n.1194+157_1194+158insACA
XM_011512866.1:c.1143+157_1143+158insACA	XP_011511168.1:n.1143+157_1143+158insACA
XM_011512867.1:c.1140+157_1140+158insACA	XP_011511169.1:n.1140+157_1140+158insACA
XM_011512868.1:c.1032+157_1032+158insACA	XP_011511170.1:n.1032+157_1032+158insACA
XM_011512869.1:c.1305+157_1305+158insACA	XP_011511171.1:n.1305+157_1305+158insACA
NM_001354663.1:c.771+157_771+158insACA	NP_001341592.1:n.771+157_771+158insACA
NM_001354664.1:c.768+157_768+158insACA	NP_001341593.1:n.768+157_768+158insACA
XR_001740158.2:n.1534+157_1534+158insACA
XR_001740159.2:n.1369+157_1369+158insACA
NM_001354663.2:c.771+157_771+158insACA	NP_001341592.1:n.771+157_771+158insACA
NM_001354664.2:c.768+157_768+158insACA	NP_001341593.1:n.768+157_768+158insACA
NM_130831.3:c.1032+157_1032+158insACA	NP_570844.1:n.1032+157_1032+158insACA
NM_130832.3:c.1086+157_1086+158insACA	NP_570845.1:n.1086+157_1086+158insACA
NM_130834.3:c.1194+157_1194+158insACA	NP_570847.2:n.1194+157_1194+158insACA
NM_130836.3:c.1251+157_1251+158insACA	NP_570849.2:n.1251+157_1251+158insACA
NM_015560.3:c.1140+157_1140+158insACA	NP_056375.2:n.1140+157_1140+158insACA
NM_130833.3:c.1143+157_1143+158insACA	NP_570846.1:n.1143+157_1143+158insACA
NM_130835.3:c.1197+157_1197+158insACA	NP_570848.1:n.1197+157_1197+158insACA
NM_130837.3:c.1305+157_1305+158insACA MANE Select	NP_570850.2:n.1305+157_1305+158insACA