Canonical Allele Identifier: CA1430243540
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193642776T= , CM000665.2:g.193642776T= GRCh38
NC_000003.11:g.193360565T= , CM000665.1:g.193360565T= GRCh37
NC_000003.10:g.194843259T= NCBI36
NG_011605.1:g.54633T= , LRG_337:g.54633T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361510.8:c.1161T= MANE Select ENSP00000355324.2:p.Ser387=
ENST00000361828.7:c.996T= ENSP00000354429.3:p.Ser332=
ENST00000361908.8:c.1107T= ENSP00000354681.3:p.Ser369=
ENST00000392436.7:c.996T= ENSP00000376231.3:p.Ser332=
ENST00000392437.6:c.1050T= ENSP00000376232.2:p.Ser350=
ENST00000642289.1:c.1080-597T=
ENST00000642445.1:c.996T= ENSP00000495535.1:p.Ser332=
ENST00000642593.1:c.996T= ENSP00000494273.1:p.Ser332=
ENST00000643329.1:c.678T= ENSP00000493673.1:p.Ser226=
ENST00000643737.1:c.*1077T= ENSP00000494210.1:n.*1077T=
ENST00000644595.1:c.996T= ENSP00000494121.1:p.Ser332=
ENST00000644629.1:c.656T=
ENST00000644841.1:c.624T= ENSP00000493988.1:p.Ser208=
ENST00000644959.1:c.965T=
ENST00000645553.1:c.1011T= ENSP00000494725.1:p.Ser337=
ENST00000646085.1:c.*474T= ENSP00000494509.1:n.*474T=
ENST00000646277.1:c.1161T= ENSP00000495289.1:p.Ser387=
ENST00000646544.1:c.59T=
ENST00000646699.1:c.1080-597T=
ENST00000646793.1:c.888T= ENSP00000494512.1:p.Ser296=
ENST00000361150.6:c.999T= ENSP00000354781.2:p.Ser333=
ENST00000361510.6:c.1161T= ENSP00000355324.2:p.Ser387=
ENST00000361715.6:c.1053T= ENSP00000355311.2:p.Ser351=
ENST00000361828.6:c.1050T= ENSP00000354429.2:p.Ser350=
ENST00000361908.7:c.1107T= ENSP00000354681.3:p.Ser369=
ENST00000392438.7:c.996T= ENSP00000376233.3:p.Ser332=
ENST00000475899.1:n.192T=
ENST00000497189.5:n.482T=
NM_015560.2:c.996T= , LRG_337t1:c.996T= NP_056375.2:p.Ser332=
NM_130831.2:c.888T= NP_570844.1:p.Ser296=
NM_130832.2:c.942T= NP_570845.1:p.Ser314=
NM_130833.2:c.999T= NP_570846.1:p.Ser333=
NM_130834.2:c.1050T= NP_570847.2:p.Ser350=
NM_130835.2:c.1053T= NP_570848.1:p.Ser351=
NM_130836.2:c.1107T= NP_570849.2:p.Ser369=
NM_130837.2:c.1161T= , LRG_337t2:c.1161T= NP_570850.2:p.Ser387=
XM_011512863.1:c.1161T= XP_011511165.1:p.Ser387=
XM_011512864.1:c.1107T= XP_011511166.1:p.Ser369=
XM_011512865.1:c.1050T= XP_011511167.1:p.Ser350=
XM_011512866.1:c.999T= XP_011511168.1:p.Ser333=
XM_011512867.1:c.996T= XP_011511169.1:p.Ser332=
XM_011512868.1:c.888T= XP_011511170.1:p.Ser296=
XM_011512869.1:c.1161T= XP_011511171.1:p.Ser387=
NM_001354663.1:c.627T= NP_001341592.1:p.Ser209=
NM_001354664.1:c.624T= NP_001341593.1:p.Ser208=
XR_001740158.2:n.1390T=
XR_001740159.2:n.1225T=
NM_001354663.2:c.627T= NP_001341592.1:p.Ser209=
NM_001354664.2:c.624T= NP_001341593.1:p.Ser208=
NM_130831.3:c.888T= NP_570844.1:p.Ser296=
NM_130832.3:c.942T= NP_570845.1:p.Ser314=
NM_130834.3:c.1050T= NP_570847.2:p.Ser350=
NM_130836.3:c.1107T= NP_570849.2:p.Ser369=
NM_015560.3:c.996T= NP_056375.2:p.Ser332=
NM_130833.3:c.999T= NP_570846.1:p.Ser333=
NM_130835.3:c.1053T= NP_570848.1:p.Ser351=
NM_130837.3:c.1161T= MANE Select NP_570850.2:p.Ser387=