Canonical Allele Identifier: CA437434551

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193355842T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193638053T>G , CM000665.2:g.193638053T>G	GRCh38
NC_000003.11:g.193355842T>G , CM000665.1:g.193355842T>G	GRCh37
NC_000003.10:g.194838536T>G	NCBI36
NG_011605.1:g.49910T>G , LRG_337:g.49910T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1137T>G MANE Select	ENSP00000355324.2:p.Arg379=
ENST00000361828.7:c.972T>G	ENSP00000354429.3:p.Arg324=
ENST00000361908.8:c.1083T>G	ENSP00000354681.3:p.Arg361=
ENST00000392436.7:c.972T>G	ENSP00000376231.3:p.Arg324=
ENST00000392437.6:c.1026T>G	ENSP00000376232.2:p.Arg342=
ENST00000642289.1:c.1067T>G
ENST00000642445.1:c.972T>G	ENSP00000495535.1:p.Arg324=
ENST00000642593.1:c.972T>G	ENSP00000494273.1:p.Arg324=
ENST00000643329.1:c.654T>G	ENSP00000493673.1:p.Arg218=
ENST00000643737.1:c.*1053T>G	ENSP00000494210.1:n.*1053T>G
ENST00000644595.1:c.972T>G	ENSP00000494121.1:p.Arg324=
ENST00000644629.1:c.632T>G
ENST00000644841.1:c.600T>G	ENSP00000493988.1:p.Arg200=
ENST00000644959.1:c.941T>G
ENST00000645553.1:c.987T>G	ENSP00000494725.1:p.Arg329=
ENST00000646085.1:c.*450T>G	ENSP00000494509.1:n.*450T>G
ENST00000646277.1:c.1137T>G	ENSP00000495289.1:p.Arg379=
ENST00000646544.1:c.35T>G
ENST00000646699.1:c.1067T>G
ENST00000646793.1:c.864T>G	ENSP00000494512.1:p.Arg288=
ENST00000361150.6:c.975T>G	ENSP00000354781.2:p.Arg325=
ENST00000361510.6:c.1137T>G	ENSP00000355324.2:p.Arg379=
ENST00000361715.6:c.1029T>G	ENSP00000355311.2:p.Arg343=
ENST00000361828.6:c.1026T>G	ENSP00000354429.2:p.Arg342=
ENST00000361908.7:c.1083T>G	ENSP00000354681.3:p.Arg361=
ENST00000392438.7:c.972T>G	ENSP00000376233.3:p.Arg324=
ENST00000475899.1:n.168T>G
ENST00000497189.5:n.458T>G
NM_015560.2:c.972T>G , LRG_337t1:c.972T>G	NP_056375.2:p.Arg324=
NM_130831.2:c.864T>G	NP_570844.1:p.Arg288=
NM_130832.2:c.918T>G	NP_570845.1:p.Arg306=
NM_130833.2:c.975T>G	NP_570846.1:p.Arg325=
NM_130834.2:c.1026T>G	NP_570847.2:p.Arg342=
NM_130835.2:c.1029T>G	NP_570848.1:p.Arg343=
NM_130836.2:c.1083T>G	NP_570849.2:p.Arg361=
NM_130837.2:c.1137T>G , LRG_337t2:c.1137T>G	NP_570850.2:p.Arg379=
XM_011512863.1:c.1137T>G	XP_011511165.1:p.Arg379=
XM_011512864.1:c.1083T>G	XP_011511166.1:p.Arg361=
XM_011512865.1:c.1026T>G	XP_011511167.1:p.Arg342=
XM_011512866.1:c.975T>G	XP_011511168.1:p.Arg325=
XM_011512867.1:c.972T>G	XP_011511169.1:p.Arg324=
XM_011512868.1:c.864T>G	XP_011511170.1:p.Arg288=
XM_011512869.1:c.1137T>G	XP_011511171.1:p.Arg379=
NM_001354663.1:c.603T>G	NP_001341592.1:p.Arg201=
NM_001354664.1:c.600T>G	NP_001341593.1:p.Arg200=
XR_001740158.2:n.1366T>G
XR_001740159.2:n.1201T>G
NM_001354663.2:c.603T>G	NP_001341592.1:p.Arg201=
NM_001354664.2:c.600T>G	NP_001341593.1:p.Arg200=
NM_130831.3:c.864T>G	NP_570844.1:p.Arg288=
NM_130832.3:c.918T>G	NP_570845.1:p.Arg306=
NM_130834.3:c.1026T>G	NP_570847.2:p.Arg342=
NM_130836.3:c.1083T>G	NP_570849.2:p.Arg361=
NM_015560.3:c.972T>G	NP_056375.2:p.Arg324=
NM_130833.3:c.975T>G	NP_570846.1:p.Arg325=
NM_130835.3:c.1029T>G	NP_570848.1:p.Arg343=
NM_130837.3:c.1137T>G MANE Select	NP_570850.2:p.Arg379=