Canonical Allele Identifier: CA2573052132

Gene: OPA1

Linked Data

• ClinVar Variation Id: 1320654
• ClinVar RCV Id: RCV001776633
• dbSNP Id: rs2109043788

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643449del , CM000665.2:g.193643449del	GRCh38
NC_000003.11:g.193361238del , CM000665.1:g.193361238del	GRCh37
NC_000003.10:g.194843932del	NCBI36
NG_011605.1:g.55306del , LRG_337:g.55306del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1377+5del MANE Select	ENSP00000355324.2:n.1377+5del
ENST00000361828.7:c.1212+5del	ENSP00000354429.3:n.1212+5del
ENST00000361908.8:c.1323+5del	ENSP00000354681.3:n.1323+5del
ENST00000392436.7:c.1212+5del	ENSP00000376231.3:n.1212+5del
ENST00000392437.6:c.1266+5del	ENSP00000376232.2:n.1266+5del
ENST00000642289.1:c.1151+5del
ENST00000642445.1:c.1212+5del	ENSP00000495535.1:n.1212+5del
ENST00000642593.1:c.1212+5del	ENSP00000494273.1:n.1212+5del
ENST00000643329.1:c.894+5del	ENSP00000493673.1:n.894+5del
ENST00000643737.1:c.*1293+5del	ENSP00000494210.1:n.*1293+5del
ENST00000644595.1:c.1212+5del	ENSP00000494121.1:n.1212+5del
ENST00000644629.1:c.872+5del
ENST00000644841.1:c.840+5del	ENSP00000493988.1:n.840+5del
ENST00000644959.1:c.1181+5del
ENST00000645553.1:c.1227+5del	ENSP00000494725.1:n.1227+5del
ENST00000646085.1:c.*690+5del	ENSP00000494509.1:n.*690+5del
ENST00000646277.1:c.1377+5del	ENSP00000495289.1:n.1377+5del
ENST00000646544.1:c.200+5del
ENST00000646699.1:c.1151+5del
ENST00000646793.1:c.1104+5del	ENSP00000494512.1:n.1104+5del
ENST00000361150.6:c.1215+5del	ENSP00000354781.2:n.1215+5del
ENST00000361510.6:c.1377+5del	ENSP00000355324.2:n.1377+5del
ENST00000361715.6:c.1269+5del	ENSP00000355311.2:n.1269+5del
ENST00000361828.6:c.1266+5del	ENSP00000354429.2:n.1266+5del
ENST00000361908.7:c.1323+5del	ENSP00000354681.3:n.1323+5del
ENST00000392438.7:c.1212+5del	ENSP00000376233.3:n.1212+5del
ENST00000475899.1:n.408+5del
NM_015560.2:c.1212+5del , LRG_337t1:c.1212+5del	NP_056375.2:n.1212+5del
NM_130831.2:c.1104+5del	NP_570844.1:n.1104+5del
NM_130832.2:c.1158+5del	NP_570845.1:n.1158+5del
NM_130833.2:c.1215+5del	NP_570846.1:n.1215+5del
NM_130834.2:c.1266+5del	NP_570847.2:n.1266+5del
NM_130835.2:c.1269+5del	NP_570848.1:n.1269+5del
NM_130836.2:c.1323+5del	NP_570849.2:n.1323+5del
NM_130837.2:c.1377+5del , LRG_337t2:c.1377+5del	NP_570850.2:n.1377+5del
XM_011512863.1:c.1377+5del	XP_011511165.1:n.1377+5del
XM_011512864.1:c.1323+5del	XP_011511166.1:n.1323+5del
XM_011512865.1:c.1266+5del	XP_011511167.1:n.1266+5del
XM_011512866.1:c.1215+5del	XP_011511168.1:n.1215+5del
XM_011512867.1:c.1212+5del	XP_011511169.1:n.1212+5del
XM_011512868.1:c.1104+5del	XP_011511170.1:n.1104+5del
XM_011512869.1:c.1377+5del	XP_011511171.1:n.1377+5del
NM_001354663.1:c.843+5del	NP_001341592.1:n.843+5del
NM_001354664.1:c.840+5del	NP_001341593.1:n.840+5del
XR_001740158.2:n.1606+5del
XR_001740159.2:n.1441+5del
NM_001354663.2:c.843+5del	NP_001341592.1:n.843+5del
NM_001354664.2:c.840+5del	NP_001341593.1:n.840+5del
NM_130831.3:c.1104+5del	NP_570844.1:n.1104+5del
NM_130832.3:c.1158+5del	NP_570845.1:n.1158+5del
NM_130834.3:c.1266+5del	NP_570847.2:n.1266+5del
NM_130836.3:c.1323+5del	NP_570849.2:n.1323+5del
NM_015560.3:c.1212+5del	NP_056375.2:n.1212+5del
NM_130833.3:c.1215+5del	NP_570846.1:n.1215+5del
NM_130835.3:c.1269+5del	NP_570848.1:n.1269+5del
NM_130837.3:c.1377+5del MANE Select	NP_570850.2:n.1377+5del