Canonical Allele Identifier: CA437441514

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377275A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659486A>G , CM000665.2:g.193659486A>G	GRCh38
NC_000003.11:g.193377275A>G , CM000665.1:g.193377275A>G	GRCh37
NC_000003.10:g.194859969A>G	NCBI36
NG_011605.1:g.71343A>G , LRG_337:g.71343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2445A>G MANE Select	ENSP00000355324.2:p.Glu815=
ENST00000361828.7:c.2280A>G	ENSP00000354429.3:p.Glu760=
ENST00000361908.8:c.2391A>G	ENSP00000354681.3:p.Glu797=
ENST00000392436.7:c.2280A>G	ENSP00000376231.3:p.Glu760=
ENST00000392437.6:c.2334A>G	ENSP00000376232.2:p.Glu778=
ENST00000642289.1:c.2219A>G
ENST00000642445.1:c.2280A>G	ENSP00000495535.1:p.Glu760=
ENST00000642593.1:c.*505A>G	ENSP00000494273.1:n.*505A>G
ENST00000643329.1:c.1962A>G	ENSP00000493673.1:p.Glu654=
ENST00000643737.1:c.*2361A>G	ENSP00000494210.1:n.*2361A>G
ENST00000644595.1:c.2280A>G	ENSP00000494121.1:p.Glu760=
ENST00000644629.1:c.1867A>G
ENST00000644841.1:c.*764A>G	ENSP00000493988.1:n.*764A>G
ENST00000644959.1:c.2274A>G
ENST00000645553.1:c.2295A>G	ENSP00000494725.1:p.Glu765=
ENST00000646085.1:c.*1758A>G	ENSP00000494509.1:n.*1758A>G
ENST00000646277.1:c.*881A>G	ENSP00000495289.1:n.*881A>G
ENST00000646544.1:c.1268A>G
ENST00000646699.1:c.2219A>G
ENST00000646793.1:c.2172A>G	ENSP00000494512.1:p.Glu724=
ENST00000361150.6:c.2283A>G	ENSP00000354781.2:p.Glu761=
ENST00000361510.6:c.2445A>G	ENSP00000355324.2:p.Glu815=
ENST00000361715.6:c.2337A>G	ENSP00000355311.2:p.Glu779=
ENST00000361828.6:c.2334A>G	ENSP00000354429.2:p.Glu778=
ENST00000361908.7:c.2391A>G	ENSP00000354681.3:p.Glu797=
ENST00000392438.7:c.2280A>G	ENSP00000376233.3:p.Glu760=
ENST00000482865.1:n.539A>G
NM_015560.2:c.2280A>G , LRG_337t1:c.2280A>G	NP_056375.2:p.Glu760=
NM_130831.2:c.2172A>G	NP_570844.1:p.Glu724=
NM_130832.2:c.2226A>G	NP_570845.1:p.Glu742=
NM_130833.2:c.2283A>G	NP_570846.1:p.Glu761=
NM_130834.2:c.2334A>G	NP_570847.2:p.Glu778=
NM_130835.2:c.2337A>G	NP_570848.1:p.Glu779=
NM_130836.2:c.2391A>G	NP_570849.2:p.Glu797=
NM_130837.2:c.2445A>G , LRG_337t2:c.2445A>G	NP_570850.2:p.Glu815=
XM_011512863.1:c.2445A>G	XP_011511165.1:p.Glu815=
XM_011512864.1:c.2391A>G	XP_011511166.1:p.Glu797=
XM_011512865.1:c.2334A>G	XP_011511167.1:p.Glu778=
XM_011512866.1:c.2283A>G	XP_011511168.1:p.Glu761=
XM_011512867.1:c.2280A>G	XP_011511169.1:p.Glu760=
XM_011512868.1:c.2172A>G	XP_011511170.1:p.Glu724=
XR_924835.1:n.582+9434T>C
NM_001354663.1:c.1911A>G	NP_001341592.1:p.Glu637=
NM_001354664.1:c.1908A>G	NP_001341593.1:p.Glu636=
XR_001740158.2:n.2699A>G
XR_001740159.2:n.2534A>G
XR_001741074.1:n.475+11322T>C
XR_924835.2:n.600+9434T>C
NM_001354663.2:c.1911A>G	NP_001341592.1:p.Glu637=
NM_001354664.2:c.1908A>G	NP_001341593.1:p.Glu636=
NM_130831.3:c.2172A>G	NP_570844.1:p.Glu724=
NM_130832.3:c.2226A>G	NP_570845.1:p.Glu742=
NM_130834.3:c.2334A>G	NP_570847.2:p.Glu778=
NM_130836.3:c.2391A>G	NP_570849.2:p.Glu797=
NM_015560.3:c.2280A>G	NP_056375.2:p.Glu760=
NM_130833.3:c.2283A>G	NP_570846.1:p.Glu761=
NM_130835.3:c.2337A>G	NP_570848.1:p.Glu779=
NM_130837.3:c.2445A>G MANE Select	NP_570850.2:p.Glu815=