Canonical Allele Identifier: CA1430233470

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193667176G= , CM000665.2:g.193667176G=	GRCh38
NC_000003.11:g.193384965G= , CM000665.1:g.193384965G=	GRCh37
NC_000003.10:g.194867659G=	NCBI36
NG_011605.1:g.79033G= , LRG_337:g.79033G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2879G= MANE Select	ENSP00000355324.2:p.Arg960=
ENST00000361828.7:c.2714G=	ENSP00000354429.3:p.Arg905=
ENST00000361908.8:c.2825G=	ENSP00000354681.3:p.Arg942=
ENST00000392436.7:c.2714G=	ENSP00000376231.3:p.Arg905=
ENST00000392437.6:c.2768G=	ENSP00000376232.2:p.Arg923=
ENST00000642289.1:c.2653G=
ENST00000642445.1:c.2714G=	ENSP00000495535.1:p.Arg905=
ENST00000642593.1:c.*939G=	ENSP00000494273.1:n.*939G=
ENST00000643329.1:c.2396G=	ENSP00000493673.1:p.Arg799=
ENST00000643737.1:c.*2795G=	ENSP00000494210.1:n.*2795G=
ENST00000644595.1:c.2714G=	ENSP00000494121.1:p.Arg905=
ENST00000644629.1:c.2301G=
ENST00000644841.1:c.*1198G=	ENSP00000493988.1:n.*1198G=
ENST00000644959.1:c.2708G=
ENST00000645553.1:c.2729G=	ENSP00000494725.1:p.Arg910=
ENST00000646085.1:c.*2192G=	ENSP00000494509.1:n.*2192G=
ENST00000646277.1:c.*1315G=	ENSP00000495289.1:n.*1315G=
ENST00000646544.1:c.1702G=
ENST00000646699.1:c.2653G=
ENST00000646793.1:c.2606G=	ENSP00000494512.1:p.Arg869=
ENST00000361150.6:c.2717G=	ENSP00000354781.2:p.Arg906=
ENST00000361510.6:c.2879G=	ENSP00000355324.2:p.Arg960=
ENST00000361715.6:c.2771G=	ENSP00000355311.2:p.Arg924=
ENST00000361828.6:c.2768G=	ENSP00000354429.2:p.Arg923=
ENST00000361908.7:c.2825G=	ENSP00000354681.3:p.Arg942=
ENST00000392438.7:c.2714G=	ENSP00000376233.3:p.Arg905=
ENST00000429164.1:c.1G=
ENST00000445863.1:c.290G=	ENSP00000398358.1:p.Arg97=
NM_015560.2:c.2714G= , LRG_337t1:c.2714G=	NP_056375.2:p.Arg905=
NM_130831.2:c.2606G=	NP_570844.1:p.Arg869=
NM_130832.2:c.2660G=	NP_570845.1:p.Arg887=
NM_130833.2:c.2717G=	NP_570846.1:p.Arg906=
NM_130834.2:c.2768G=	NP_570847.2:p.Arg923=
NM_130835.2:c.2771G=	NP_570848.1:p.Arg924=
NM_130836.2:c.2825G=	NP_570849.2:p.Arg942=
NM_130837.2:c.2879G= , LRG_337t2:c.2879G=	NP_570850.2:p.Arg960=
XM_011512863.1:c.2879G=	XP_011511165.1:p.Arg960=
XM_011512864.1:c.2825G=	XP_011511166.1:p.Arg942=
XM_011512865.1:c.2768G=	XP_011511167.1:p.Arg923=
XM_011512866.1:c.2717G=	XP_011511168.1:p.Arg906=
XM_011512867.1:c.2714G=	XP_011511169.1:p.Arg905=
XM_011512868.1:c.2606G=	XP_011511170.1:p.Arg869=
XR_924835.1:n.582+1744C=
NM_001354663.1:c.2345G=	NP_001341592.1:p.Arg782=
NM_001354664.1:c.2342G=	NP_001341593.1:p.Arg781=
XR_001740158.2:n.3133G=
XR_001740159.2:n.2968G=
XR_001741072.1:n.600+1744C=
XR_001741074.1:n.475+3632C=
XR_924835.2:n.600+1744C=
NM_001354663.2:c.2345G=	NP_001341592.1:p.Arg782=
NM_001354664.2:c.2342G=	NP_001341593.1:p.Arg781=
NM_130831.3:c.2606G=	NP_570844.1:p.Arg869=
NM_130832.3:c.2660G=	NP_570845.1:p.Arg887=
NM_130834.3:c.2768G=	NP_570847.2:p.Arg923=
NM_130836.3:c.2825G=	NP_570849.2:p.Arg942=
NM_015560.3:c.2714G=	NP_056375.2:p.Arg905=
NM_130833.3:c.2717G=	NP_570846.1:p.Arg906=
NM_130835.3:c.2771G=	NP_570848.1:p.Arg924=
NM_130837.3:c.2879G= MANE Select	NP_570850.2:p.Arg960=