Canonical Allele Identifier: CA1430270692

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662920G= , CM000665.2:g.193662920G=	GRCh38
NC_000003.11:g.193380709G= , CM000665.1:g.193380709G=	GRCh37
NC_000003.10:g.194863403G=	NCBI36
NG_011605.1:g.74777G= , LRG_337:g.74777G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2619G= MANE Select	ENSP00000355324.2:p.Arg873=
ENST00000361828.7:c.2454G=	ENSP00000354429.3:p.Arg818=
ENST00000361908.8:c.2565G=	ENSP00000354681.3:p.Arg855=
ENST00000392436.7:c.2454G=	ENSP00000376231.3:p.Arg818=
ENST00000392437.6:c.2508G=	ENSP00000376232.2:p.Arg836=
ENST00000642289.1:c.2393G=
ENST00000642445.1:c.2454G=	ENSP00000495535.1:p.Arg818=
ENST00000642593.1:c.*679G=	ENSP00000494273.1:n.*679G=
ENST00000643329.1:c.2136G=	ENSP00000493673.1:p.Arg712=
ENST00000643737.1:c.*2535G=	ENSP00000494210.1:n.*2535G=
ENST00000644595.1:c.2454G=	ENSP00000494121.1:p.Arg818=
ENST00000644629.1:c.2041G=
ENST00000644841.1:c.*938G=	ENSP00000493988.1:n.*938G=
ENST00000644959.1:c.2448G=
ENST00000645553.1:c.2469G=	ENSP00000494725.1:p.Arg823=
ENST00000646085.1:c.*1932G=	ENSP00000494509.1:n.*1932G=
ENST00000646277.1:c.*1055G=	ENSP00000495289.1:n.*1055G=
ENST00000646544.1:c.1442G=
ENST00000646699.1:c.2393G=
ENST00000646793.1:c.2346G=	ENSP00000494512.1:p.Arg782=
ENST00000361150.6:c.2457G=	ENSP00000354781.2:p.Arg819=
ENST00000361510.6:c.2619G=	ENSP00000355324.2:p.Arg873=
ENST00000361715.6:c.2511G=	ENSP00000355311.2:p.Arg837=
ENST00000361828.6:c.2508G=	ENSP00000354429.2:p.Arg836=
ENST00000361908.7:c.2565G=	ENSP00000354681.3:p.Arg855=
ENST00000392438.7:c.2454G=	ENSP00000376233.3:p.Arg818=
ENST00000445863.1:c.30G=	ENSP00000398358.1:p.Arg10=
NM_015560.2:c.2454G= , LRG_337t1:c.2454G=	NP_056375.2:p.Arg818=
NM_130831.2:c.2346G=	NP_570844.1:p.Arg782=
NM_130832.2:c.2400G=	NP_570845.1:p.Arg800=
NM_130833.2:c.2457G=	NP_570846.1:p.Arg819=
NM_130834.2:c.2508G=	NP_570847.2:p.Arg836=
NM_130835.2:c.2511G=	NP_570848.1:p.Arg837=
NM_130836.2:c.2565G=	NP_570849.2:p.Arg855=
NM_130837.2:c.2619G= , LRG_337t2:c.2619G=	NP_570850.2:p.Arg873=
XM_011512863.1:c.2619G=	XP_011511165.1:p.Arg873=
XM_011512864.1:c.2565G=	XP_011511166.1:p.Arg855=
XM_011512865.1:c.2508G=	XP_011511167.1:p.Arg836=
XM_011512866.1:c.2457G=	XP_011511168.1:p.Arg819=
XM_011512867.1:c.2454G=	XP_011511169.1:p.Arg818=
XM_011512868.1:c.2346G=	XP_011511170.1:p.Arg782=
XR_924835.1:n.582+6000C=
NM_001354663.1:c.2085G=	NP_001341592.1:p.Arg695=
NM_001354664.1:c.2082G=	NP_001341593.1:p.Arg694=
XR_001740158.2:n.2873G=
XR_001740159.2:n.2708G=
XR_001741072.1:n.601-2835C=
XR_001741074.1:n.475+7888C=
XR_924835.2:n.600+6000C=
NM_001354663.2:c.2085G=	NP_001341592.1:p.Arg695=
NM_001354664.2:c.2082G=	NP_001341593.1:p.Arg694=
NM_130831.3:c.2346G=	NP_570844.1:p.Arg782=
NM_130832.3:c.2400G=	NP_570845.1:p.Arg800=
NM_130834.3:c.2508G=	NP_570847.2:p.Arg836=
NM_130836.3:c.2565G=	NP_570849.2:p.Arg855=
NM_015560.3:c.2454G=	NP_056375.2:p.Arg818=
NM_130833.3:c.2457G=	NP_570846.1:p.Arg819=
NM_130835.3:c.2511G=	NP_570848.1:p.Arg837=
NM_130837.3:c.2619G= MANE Select	NP_570850.2:p.Arg873=