Canonical Allele Identifier: CA2586973450

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643444del , CM000665.2:g.193643444del	GRCh38
NC_000003.11:g.193361233del , CM000665.1:g.193361233del	GRCh37
NC_000003.10:g.194843927del	NCBI36
NG_011605.1:g.55301del , LRG_337:g.55301del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1377del MANE Select	ENSP00000355324.2:p.Asn459LysfsTer3
ENST00000361828.7:c.1212del	ENSP00000354429.3:p.Asn404LysfsTer3
ENST00000361908.8:c.1323del	ENSP00000354681.3:p.Asn441LysfsTer3
ENST00000392436.7:c.1212del	ENSP00000376231.3:p.Asn404LysfsTer3
ENST00000392437.6:c.1266del	ENSP00000376232.2:p.Asn422LysfsTer3
ENST00000642289.1:c.1151del
ENST00000642445.1:c.1212del	ENSP00000495535.1:p.Asn404LysfsTer3
ENST00000642593.1:c.1212del	ENSP00000494273.1:p.Asn404LysfsTer3
ENST00000643329.1:c.894del	ENSP00000493673.1:p.Asn298LysfsTer3
ENST00000643737.1:c.*1293del	ENSP00000494210.1:n.*1293del
ENST00000644595.1:c.1212del	ENSP00000494121.1:p.Asn404LysfsTer3
ENST00000644629.1:c.872del
ENST00000644841.1:c.840del	ENSP00000493988.1:p.Asn280LysfsTer3
ENST00000644959.1:c.1181del
ENST00000645553.1:c.1227del	ENSP00000494725.1:p.Asn409LysfsTer3
ENST00000646085.1:c.*690del	ENSP00000494509.1:n.*690del
ENST00000646277.1:c.1377del	ENSP00000495289.1:p.Asn459LysfsTer3
ENST00000646544.1:c.200del
ENST00000646699.1:c.1151del
ENST00000646793.1:c.1104del	ENSP00000494512.1:p.Asn368LysfsTer3
ENST00000361150.6:c.1215del	ENSP00000354781.2:p.Asn405LysfsTer3
ENST00000361510.6:c.1377del	ENSP00000355324.2:p.Asn459LysfsTer3
ENST00000361715.6:c.1269del	ENSP00000355311.2:p.Asn423LysfsTer3
ENST00000361828.6:c.1266del	ENSP00000354429.2:p.Asn422LysfsTer3
ENST00000361908.7:c.1323del	ENSP00000354681.3:p.Asn441LysfsTer3
ENST00000392438.7:c.1212del	ENSP00000376233.3:p.Asn404LysfsTer3
ENST00000475899.1:n.408del
NM_015560.2:c.1212del , LRG_337t1:c.1212del	NP_056375.2:p.Asn404LysfsTer3
NM_130831.2:c.1104del	NP_570844.1:p.Asn368LysfsTer3
NM_130832.2:c.1158del	NP_570845.1:p.Asn386LysfsTer3
NM_130833.2:c.1215del	NP_570846.1:p.Asn405LysfsTer3
NM_130834.2:c.1266del	NP_570847.2:p.Asn422LysfsTer3
NM_130835.2:c.1269del	NP_570848.1:p.Asn423LysfsTer3
NM_130836.2:c.1323del	NP_570849.2:p.Asn441LysfsTer3
NM_130837.2:c.1377del , LRG_337t2:c.1377del	NP_570850.2:p.Asn459LysfsTer3
XM_011512863.1:c.1377del	XP_011511165.1:p.Asn459LysfsTer3
XM_011512864.1:c.1323del	XP_011511166.1:p.Asn441LysfsTer3
XM_011512865.1:c.1266del	XP_011511167.1:p.Asn422LysfsTer3
XM_011512866.1:c.1215del	XP_011511168.1:p.Asn405LysfsTer3
XM_011512867.1:c.1212del	XP_011511169.1:p.Asn404LysfsTer3
XM_011512868.1:c.1104del	XP_011511170.1:p.Asn368LysfsTer3
XM_011512869.1:c.1377del	XP_011511171.1:p.Asn459LysfsTer3
NM_001354663.1:c.843del	NP_001341592.1:p.Asn281LysfsTer3
NM_001354664.1:c.840del	NP_001341593.1:p.Asn280LysfsTer3
XR_001740158.2:n.1606del
XR_001740159.2:n.1441del
NM_001354663.2:c.843del	NP_001341592.1:p.Asn281LysfsTer3
NM_001354664.2:c.840del	NP_001341593.1:p.Asn280LysfsTer3
NM_130831.3:c.1104del	NP_570844.1:p.Asn368LysfsTer3
NM_130832.3:c.1158del	NP_570845.1:p.Asn386LysfsTer3
NM_130834.3:c.1266del	NP_570847.2:p.Asn422LysfsTer3
NM_130836.3:c.1323del	NP_570849.2:p.Asn441LysfsTer3
NM_015560.3:c.1212del	NP_056375.2:p.Asn404LysfsTer3
NM_130833.3:c.1215del	NP_570846.1:p.Asn405LysfsTer3
NM_130835.3:c.1269del	NP_570848.1:p.Asn423LysfsTer3
NM_130837.3:c.1377del MANE Select	NP_570850.2:p.Asn459LysfsTer3