Canonical Allele Identifier: CA355788216

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193355763G>C (hg19) ; chr3:g.193637974G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193637974G>C , CM000665.2:g.193637974G>C	GRCh38
NC_000003.11:g.193355763G>C , CM000665.1:g.193355763G>C	GRCh37
NC_000003.10:g.194838457G>C	NCBI36
NG_011605.1:g.49831G>C , LRG_337:g.49831G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1058G>C MANE Select	ENSP00000355324.2:p.Ser353Thr
ENST00000361828.7:c.893G>C	ENSP00000354429.3:p.Ser298Thr
ENST00000361908.8:c.1004G>C	ENSP00000354681.3:p.Ser335Thr
ENST00000392436.7:c.893G>C	ENSP00000376231.3:p.Ser298Thr
ENST00000392437.6:c.947G>C	ENSP00000376232.2:p.Ser316Thr
ENST00000642289.1:c.988G>C
ENST00000642445.1:c.893G>C	ENSP00000495535.1:p.Ser298Thr
ENST00000642593.1:c.893G>C	ENSP00000494273.1:p.Ser298Thr
ENST00000643329.1:c.575G>C	ENSP00000493673.1:p.Ser192Thr
ENST00000643737.1:c.*974G>C	ENSP00000494210.1:n.*974G>C
ENST00000644595.1:c.893G>C	ENSP00000494121.1:p.Ser298Thr
ENST00000644629.1:c.553G>C
ENST00000644841.1:c.521G>C	ENSP00000493988.1:p.Ser174Thr
ENST00000644959.1:c.862G>C
ENST00000645553.1:c.908G>C	ENSP00000494725.1:p.Ser303Thr
ENST00000646085.1:c.*371G>C	ENSP00000494509.1:n.*371G>C
ENST00000646277.1:c.1058G>C	ENSP00000495289.1:p.Ser353Thr
ENST00000646699.1:c.988G>C
ENST00000646793.1:c.785G>C	ENSP00000494512.1:p.Ser262Thr
ENST00000361150.6:c.896G>C	ENSP00000354781.2:p.Ser299Thr
ENST00000361510.6:c.1058G>C	ENSP00000355324.2:p.Ser353Thr
ENST00000361715.6:c.950G>C	ENSP00000355311.2:p.Ser317Thr
ENST00000361828.6:c.947G>C	ENSP00000354429.2:p.Ser316Thr
ENST00000361908.7:c.1004G>C	ENSP00000354681.3:p.Ser335Thr
ENST00000392438.7:c.893G>C	ENSP00000376233.3:p.Ser298Thr
ENST00000475899.1:n.89G>C
ENST00000495476.1:n.414G>C
ENST00000497189.5:n.379G>C
NM_015560.2:c.893G>C , LRG_337t1:c.893G>C	NP_056375.2:p.Ser298Thr
NM_130831.2:c.785G>C	NP_570844.1:p.Ser262Thr
NM_130832.2:c.839G>C	NP_570845.1:p.Ser280Thr
NM_130833.2:c.896G>C	NP_570846.1:p.Ser299Thr
NM_130834.2:c.947G>C	NP_570847.2:p.Ser316Thr
NM_130835.2:c.950G>C	NP_570848.1:p.Ser317Thr
NM_130836.2:c.1004G>C	NP_570849.2:p.Ser335Thr
NM_130837.2:c.1058G>C , LRG_337t2:c.1058G>C	NP_570850.2:p.Ser353Thr
XM_011512863.1:c.1058G>C	XP_011511165.1:p.Ser353Thr
XM_011512864.1:c.1004G>C	XP_011511166.1:p.Ser335Thr
XM_011512865.1:c.947G>C	XP_011511167.1:p.Ser316Thr
XM_011512866.1:c.896G>C	XP_011511168.1:p.Ser299Thr
XM_011512867.1:c.893G>C	XP_011511169.1:p.Ser298Thr
XM_011512868.1:c.785G>C	XP_011511170.1:p.Ser262Thr
XM_011512869.1:c.1058G>C	XP_011511171.1:p.Ser353Thr
NM_001354663.1:c.524G>C	NP_001341592.1:p.Ser175Thr
NM_001354664.1:c.521G>C	NP_001341593.1:p.Ser174Thr
XR_001740158.2:n.1287G>C
XR_001740159.2:n.1122G>C
NM_001354663.2:c.524G>C	NP_001341592.1:p.Ser175Thr
NM_001354664.2:c.521G>C	NP_001341593.1:p.Ser174Thr
NM_130831.3:c.785G>C	NP_570844.1:p.Ser262Thr
NM_130832.3:c.839G>C	NP_570845.1:p.Ser280Thr
NM_130834.3:c.947G>C	NP_570847.2:p.Ser316Thr
NM_130836.3:c.1004G>C	NP_570849.2:p.Ser335Thr
NM_015560.3:c.893G>C	NP_056375.2:p.Ser298Thr
NM_130833.3:c.896G>C	NP_570846.1:p.Ser299Thr
NM_130835.3:c.950G>C	NP_570848.1:p.Ser317Thr
NM_130837.3:c.1058G>C MANE Select	NP_570850.2:p.Ser353Thr