Canonical Allele Identifier: CA355788813

Gene: OPA1

Linked Data

• gnomAD v4: 3-193642780-G-T
• MyVariant Identifiers: chr3:g.193360569G>T (hg19) ; chr3:g.193642780G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193642780G>T , CM000665.2:g.193642780G>T	GRCh38
NC_000003.11:g.193360569G>T , CM000665.1:g.193360569G>T	GRCh37
NC_000003.10:g.194843263G>T	NCBI36
NG_011605.1:g.54637G>T , LRG_337:g.54637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1165G>T MANE Select	ENSP00000355324.2:p.Gly389Cys
ENST00000361828.7:c.1000G>T	ENSP00000354429.3:p.Gly334Cys
ENST00000361908.8:c.1111G>T	ENSP00000354681.3:p.Gly371Cys
ENST00000392436.7:c.1000G>T	ENSP00000376231.3:p.Gly334Cys
ENST00000392437.6:c.1054G>T	ENSP00000376232.2:p.Gly352Cys
ENST00000642289.1:c.1080-593G>T
ENST00000642445.1:c.1000G>T	ENSP00000495535.1:p.Gly334Cys
ENST00000642593.1:c.1000G>T	ENSP00000494273.1:p.Gly334Cys
ENST00000643329.1:c.682G>T	ENSP00000493673.1:p.Gly228Cys
ENST00000643737.1:c.*1081G>T	ENSP00000494210.1:n.*1081G>T
ENST00000644595.1:c.1000G>T	ENSP00000494121.1:p.Gly334Cys
ENST00000644629.1:c.660G>T
ENST00000644841.1:c.628G>T	ENSP00000493988.1:p.Gly210Cys
ENST00000644959.1:c.969G>T
ENST00000645553.1:c.1015G>T	ENSP00000494725.1:p.Gly339Cys
ENST00000646085.1:c.*478G>T	ENSP00000494509.1:n.*478G>T
ENST00000646277.1:c.1165G>T	ENSP00000495289.1:p.Gly389Cys
ENST00000646544.1:c.63G>T
ENST00000646699.1:c.1080-593G>T
ENST00000646793.1:c.892G>T	ENSP00000494512.1:p.Gly298Cys
ENST00000361150.6:c.1003G>T	ENSP00000354781.2:p.Gly335Cys
ENST00000361510.6:c.1165G>T	ENSP00000355324.2:p.Gly389Cys
ENST00000361715.6:c.1057G>T	ENSP00000355311.2:p.Gly353Cys
ENST00000361828.6:c.1054G>T	ENSP00000354429.2:p.Gly352Cys
ENST00000361908.7:c.1111G>T	ENSP00000354681.3:p.Gly371Cys
ENST00000392438.7:c.1000G>T	ENSP00000376233.3:p.Gly334Cys
ENST00000475899.1:n.196G>T
ENST00000497189.5:n.486G>T
NM_015560.2:c.1000G>T , LRG_337t1:c.1000G>T	NP_056375.2:p.Gly334Cys
NM_130831.2:c.892G>T	NP_570844.1:p.Gly298Cys
NM_130832.2:c.946G>T	NP_570845.1:p.Gly316Cys
NM_130833.2:c.1003G>T	NP_570846.1:p.Gly335Cys
NM_130834.2:c.1054G>T	NP_570847.2:p.Gly352Cys
NM_130835.2:c.1057G>T	NP_570848.1:p.Gly353Cys
NM_130836.2:c.1111G>T	NP_570849.2:p.Gly371Cys
NM_130837.2:c.1165G>T , LRG_337t2:c.1165G>T	NP_570850.2:p.Gly389Cys
XM_011512863.1:c.1165G>T	XP_011511165.1:p.Gly389Cys
XM_011512864.1:c.1111G>T	XP_011511166.1:p.Gly371Cys
XM_011512865.1:c.1054G>T	XP_011511167.1:p.Gly352Cys
XM_011512866.1:c.1003G>T	XP_011511168.1:p.Gly335Cys
XM_011512867.1:c.1000G>T	XP_011511169.1:p.Gly334Cys
XM_011512868.1:c.892G>T	XP_011511170.1:p.Gly298Cys
XM_011512869.1:c.1165G>T	XP_011511171.1:p.Gly389Cys
NM_001354663.1:c.631G>T	NP_001341592.1:p.Gly211Cys
NM_001354664.1:c.628G>T	NP_001341593.1:p.Gly210Cys
XR_001740158.2:n.1394G>T
XR_001740159.2:n.1229G>T
NM_001354663.2:c.631G>T	NP_001341592.1:p.Gly211Cys
NM_001354664.2:c.628G>T	NP_001341593.1:p.Gly210Cys
NM_130831.3:c.892G>T	NP_570844.1:p.Gly298Cys
NM_130832.3:c.946G>T	NP_570845.1:p.Gly316Cys
NM_130834.3:c.1054G>T	NP_570847.2:p.Gly352Cys
NM_130836.3:c.1111G>T	NP_570849.2:p.Gly371Cys
NM_015560.3:c.1000G>T	NP_056375.2:p.Gly334Cys
NM_130833.3:c.1003G>T	NP_570846.1:p.Gly335Cys
NM_130835.3:c.1057G>T	NP_570848.1:p.Gly353Cys
NM_130837.3:c.1165G>T MANE Select	NP_570850.2:p.Gly389Cys