Canonical Allele Identifier: CA1430250735

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647145G= , CM000665.2:g.193647145G=	GRCh38
NC_000003.11:g.193364934G= , CM000665.1:g.193364934G=	GRCh37
NC_000003.10:g.194847628G=	NCBI36
NG_011605.1:g.59002G= , LRG_337:g.59002G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1835G= MANE Select	ENSP00000355324.2:p.Arg612=
ENST00000361828.7:c.1670G=	ENSP00000354429.3:p.Arg557=
ENST00000361908.8:c.1781G=	ENSP00000354681.3:p.Arg594=
ENST00000392436.7:c.1670G=	ENSP00000376231.3:p.Arg557=
ENST00000392437.6:c.1724G=	ENSP00000376232.2:p.Arg575=
ENST00000642289.1:c.1609G=
ENST00000642445.1:c.1670G=	ENSP00000495535.1:p.Arg557=
ENST00000642593.1:c.1670G=	ENSP00000494273.1:p.Arg557=
ENST00000643329.1:c.1352G=	ENSP00000493673.1:p.Arg451=
ENST00000643737.1:c.*1751G=	ENSP00000494210.1:n.*1751G=
ENST00000644595.1:c.1670G=	ENSP00000494121.1:p.Arg557=
ENST00000644629.1:c.1257G=
ENST00000644841.1:c.*154G=	ENSP00000493988.1:n.*154G=
ENST00000644959.1:c.1639G=
ENST00000645553.1:c.1685G=	ENSP00000494725.1:p.Arg562=
ENST00000646085.1:c.*1148G=	ENSP00000494509.1:n.*1148G=
ENST00000646277.1:c.*271G=	ENSP00000495289.1:n.*271G=
ENST00000646544.1:c.658G=
ENST00000646699.1:c.1609G=
ENST00000646793.1:c.1562G=	ENSP00000494512.1:p.Arg521=
ENST00000361150.6:c.1673G=	ENSP00000354781.2:p.Arg558=
ENST00000361510.6:c.1835G=	ENSP00000355324.2:p.Arg612=
ENST00000361715.6:c.1727G=	ENSP00000355311.2:p.Arg576=
ENST00000361828.6:c.1724G=	ENSP00000354429.2:p.Arg575=
ENST00000361908.7:c.1781G=	ENSP00000354681.3:p.Arg594=
ENST00000392438.7:c.1670G=	ENSP00000376233.3:p.Arg557=
ENST00000483516.1:n.168G=
NM_015560.2:c.1670G= , LRG_337t1:c.1670G=	NP_056375.2:p.Arg557=
NM_130831.2:c.1562G=	NP_570844.1:p.Arg521=
NM_130832.2:c.1616G=	NP_570845.1:p.Arg539=
NM_130833.2:c.1673G=	NP_570846.1:p.Arg558=
NM_130834.2:c.1724G=	NP_570847.2:p.Arg575=
NM_130835.2:c.1727G=	NP_570848.1:p.Arg576=
NM_130836.2:c.1781G=	NP_570849.2:p.Arg594=
NM_130837.2:c.1835G= , LRG_337t2:c.1835G=	NP_570850.2:p.Arg612=
XM_011512863.1:c.1835G=	XP_011511165.1:p.Arg612=
XM_011512864.1:c.1781G=	XP_011511166.1:p.Arg594=
XM_011512865.1:c.1724G=	XP_011511167.1:p.Arg575=
XM_011512866.1:c.1673G=	XP_011511168.1:p.Arg558=
XM_011512867.1:c.1670G=	XP_011511169.1:p.Arg557=
XM_011512868.1:c.1562G=	XP_011511170.1:p.Arg521=
XM_011512869.1:c.1835G=	XP_011511171.1:p.Arg612=
NM_001354663.1:c.1301G=	NP_001341592.1:p.Arg434=
NM_001354664.1:c.1298G=	NP_001341593.1:p.Arg433=
XR_001740158.2:n.2064G=
XR_001740159.2:n.1899G=
NM_001354663.2:c.1301G=	NP_001341592.1:p.Arg434=
NM_001354664.2:c.1298G=	NP_001341593.1:p.Arg433=
NM_130831.3:c.1562G=	NP_570844.1:p.Arg521=
NM_130832.3:c.1616G=	NP_570845.1:p.Arg539=
NM_130834.3:c.1724G=	NP_570847.2:p.Arg575=
NM_130836.3:c.1781G=	NP_570849.2:p.Arg594=
NM_015560.3:c.1670G=	NP_056375.2:p.Arg557=
NM_130833.3:c.1673G=	NP_570846.1:p.Arg558=
NM_130835.3:c.1727G=	NP_570848.1:p.Arg576=
NM_130837.3:c.1835G= MANE Select	NP_570850.2:p.Arg612=