Canonical Allele Identifier: CA2759297

Gene: OPA1

Linked Data

• dbSNP Id: rs764775588
• ExAC: 3:193360605 C / T
• gnomAD v2: 3-193360605-C-T
• gnomAD v4: 3-193642816-C-T
• MyVariant Identifiers: chr3:g.193360605C>T (hg19) ; chr3:g.193642816C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193642816C>T , CM000665.2:g.193642816C>T	GRCh38
NC_000003.11:g.193360605C>T , CM000665.1:g.193360605C>T	GRCh37
NC_000003.10:g.194843299C>T	NCBI36
NG_011605.1:g.54673C>T , LRG_337:g.54673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1201C>T MANE Select	ENSP00000355324.2:p.Arg401Trp
ENST00000361828.7:c.1036C>T	ENSP00000354429.3:p.Arg346Trp
ENST00000361908.8:c.1147C>T	ENSP00000354681.3:p.Arg383Trp
ENST00000392436.7:c.1036C>T	ENSP00000376231.3:p.Arg346Trp
ENST00000392437.6:c.1090C>T	ENSP00000376232.2:p.Arg364Trp
ENST00000642289.1:c.1080-557C>T
ENST00000642445.1:c.1036C>T	ENSP00000495535.1:p.Arg346Trp
ENST00000642593.1:c.1036C>T	ENSP00000494273.1:p.Arg346Trp
ENST00000643329.1:c.718C>T	ENSP00000493673.1:p.Arg240Trp
ENST00000643737.1:c.*1117C>T	ENSP00000494210.1:n.*1117C>T
ENST00000644595.1:c.1036C>T	ENSP00000494121.1:p.Arg346Trp
ENST00000644629.1:c.696C>T
ENST00000644841.1:c.664C>T	ENSP00000493988.1:p.Arg222Trp
ENST00000644959.1:c.1005C>T
ENST00000645553.1:c.1051C>T	ENSP00000494725.1:p.Arg351Trp
ENST00000646085.1:c.*514C>T	ENSP00000494509.1:n.*514C>T
ENST00000646277.1:c.1201C>T	ENSP00000495289.1:p.Arg401Trp
ENST00000646544.1:c.99C>T
ENST00000646699.1:c.1080-557C>T
ENST00000646793.1:c.928C>T	ENSP00000494512.1:p.Arg310Trp
ENST00000361150.6:c.1039C>T	ENSP00000354781.2:p.Arg347Trp
ENST00000361510.6:c.1201C>T	ENSP00000355324.2:p.Arg401Trp
ENST00000361715.6:c.1093C>T	ENSP00000355311.2:p.Arg365Trp
ENST00000361828.6:c.1090C>T	ENSP00000354429.2:p.Arg364Trp
ENST00000361908.7:c.1147C>T	ENSP00000354681.3:p.Arg383Trp
ENST00000392438.7:c.1036C>T	ENSP00000376233.3:p.Arg346Trp
ENST00000475899.1:n.232C>T
ENST00000497189.5:n.522C>T
NM_015560.2:c.1036C>T , LRG_337t1:c.1036C>T	NP_056375.2:p.Arg346Trp
NM_130831.2:c.928C>T	NP_570844.1:p.Arg310Trp
NM_130832.2:c.982C>T	NP_570845.1:p.Arg328Trp
NM_130833.2:c.1039C>T	NP_570846.1:p.Arg347Trp
NM_130834.2:c.1090C>T	NP_570847.2:p.Arg364Trp
NM_130835.2:c.1093C>T	NP_570848.1:p.Arg365Trp
NM_130836.2:c.1147C>T	NP_570849.2:p.Arg383Trp
NM_130837.2:c.1201C>T , LRG_337t2:c.1201C>T	NP_570850.2:p.Arg401Trp
XM_011512863.1:c.1201C>T	XP_011511165.1:p.Arg401Trp
XM_011512864.1:c.1147C>T	XP_011511166.1:p.Arg383Trp
XM_011512865.1:c.1090C>T	XP_011511167.1:p.Arg364Trp
XM_011512866.1:c.1039C>T	XP_011511168.1:p.Arg347Trp
XM_011512867.1:c.1036C>T	XP_011511169.1:p.Arg346Trp
XM_011512868.1:c.928C>T	XP_011511170.1:p.Arg310Trp
XM_011512869.1:c.1201C>T	XP_011511171.1:p.Arg401Trp
NM_001354663.1:c.667C>T	NP_001341592.1:p.Arg223Trp
NM_001354664.1:c.664C>T	NP_001341593.1:p.Arg222Trp
XR_001740158.2:n.1430C>T
XR_001740159.2:n.1265C>T
NM_001354663.2:c.667C>T	NP_001341592.1:p.Arg223Trp
NM_001354664.2:c.664C>T	NP_001341593.1:p.Arg222Trp
NM_130831.3:c.928C>T	NP_570844.1:p.Arg310Trp
NM_130832.3:c.982C>T	NP_570845.1:p.Arg328Trp
NM_130834.3:c.1090C>T	NP_570847.2:p.Arg364Trp
NM_130836.3:c.1147C>T	NP_570849.2:p.Arg383Trp
NM_015560.3:c.1036C>T	NP_056375.2:p.Arg346Trp
NM_130833.3:c.1039C>T	NP_570846.1:p.Arg347Trp
NM_130835.3:c.1093C>T	NP_570848.1:p.Arg365Trp
NM_130837.3:c.1201C>T MANE Select	NP_570850.2:p.Arg401Trp