Canonical Allele Identifier: CA1430252005
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193648114C= , CM000665.2:g.193648114C= GRCh38
NC_000003.11:g.193365903C= , CM000665.1:g.193365903C= GRCh37
NC_000003.10:g.194848597C= NCBI36
NG_011605.1:g.59971C= , LRG_337:g.59971C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361510.8:c.1915C= MANE Select ENSP00000355324.2:p.Arg639=
ENST00000361828.7:c.1750C= ENSP00000354429.3:p.Arg584=
ENST00000361908.8:c.1861C= ENSP00000354681.3:p.Arg621=
ENST00000392436.7:c.1750C= ENSP00000376231.3:p.Arg584=
ENST00000392437.6:c.1804C= ENSP00000376232.2:p.Arg602=
ENST00000642289.1:c.1689C=
ENST00000642445.1:c.1750C= ENSP00000495535.1:p.Arg584=
ENST00000642593.1:c.1706-681C= ENSP00000494273.1:n.1706-681C=
ENST00000643329.1:c.1432C= ENSP00000493673.1:p.Arg478=
ENST00000643737.1:c.*1831C= ENSP00000494210.1:n.*1831C=
ENST00000644595.1:c.1750C= ENSP00000494121.1:p.Arg584=
ENST00000644629.1:c.1337C=
ENST00000644841.1:c.*234C= ENSP00000493988.1:n.*234C=
ENST00000644959.1:c.1719C=
ENST00000645553.1:c.1765C= ENSP00000494725.1:p.Arg589=
ENST00000646085.1:c.*1228C= ENSP00000494509.1:n.*1228C=
ENST00000646277.1:c.*351C= ENSP00000495289.1:n.*351C=
ENST00000646544.1:c.738C=
ENST00000646699.1:c.1689C=
ENST00000646793.1:c.1642C= ENSP00000494512.1:p.Arg548=
ENST00000361150.6:c.1753C= ENSP00000354781.2:p.Arg585=
ENST00000361510.6:c.1915C= ENSP00000355324.2:p.Arg639=
ENST00000361715.6:c.1807C= ENSP00000355311.2:p.Arg603=
ENST00000361828.6:c.1804C= ENSP00000354429.2:p.Arg602=
ENST00000361908.7:c.1861C= ENSP00000354681.3:p.Arg621=
ENST00000392438.7:c.1750C= ENSP00000376233.3:p.Arg584=
ENST00000483516.1:n.248C=
NM_015560.2:c.1750C= , LRG_337t1:c.1750C= NP_056375.2:p.Arg584=
NM_130831.2:c.1642C= NP_570844.1:p.Arg548=
NM_130832.2:c.1696C= NP_570845.1:p.Arg566=
NM_130833.2:c.1753C= NP_570846.1:p.Arg585=
NM_130834.2:c.1804C= NP_570847.2:p.Arg602=
NM_130835.2:c.1807C= NP_570848.1:p.Arg603=
NM_130836.2:c.1861C= NP_570849.2:p.Arg621=
NM_130837.2:c.1915C= , LRG_337t2:c.1915C= NP_570850.2:p.Arg639=
XM_011512863.1:c.1915C= XP_011511165.1:p.Arg639=
XM_011512864.1:c.1861C= XP_011511166.1:p.Arg621=
XM_011512865.1:c.1804C= XP_011511167.1:p.Arg602=
XM_011512866.1:c.1753C= XP_011511168.1:p.Arg585=
XM_011512867.1:c.1750C= XP_011511169.1:p.Arg584=
XM_011512868.1:c.1642C= XP_011511170.1:p.Arg548=
XM_011512869.1:c.1915C= XP_011511171.1:p.Arg639=
XR_924835.1:n.583-804G=
NM_001354663.1:c.1381C= NP_001341592.1:p.Arg461=
NM_001354664.1:c.1378C= NP_001341593.1:p.Arg460=
XR_001740158.2:n.2144C=
XR_001740159.2:n.1979C=
XR_001741074.1:n.476-804G=
XR_924835.2:n.601-804G=
NM_001354663.2:c.1381C= NP_001341592.1:p.Arg461=
NM_001354664.2:c.1378C= NP_001341593.1:p.Arg460=
NM_130831.3:c.1642C= NP_570844.1:p.Arg548=
NM_130832.3:c.1696C= NP_570845.1:p.Arg566=
NM_130834.3:c.1804C= NP_570847.2:p.Arg602=
NM_130836.3:c.1861C= NP_570849.2:p.Arg621=
NM_015560.3:c.1750C= NP_056375.2:p.Arg584=
NM_130833.3:c.1753C= NP_570846.1:p.Arg585=
NM_130835.3:c.1807C= NP_570848.1:p.Arg603=
NM_130837.3:c.1915C= MANE Select NP_570850.2:p.Arg639=