Canonical Allele Identifier: CA437435618

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193360622C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193642833C>G , CM000665.2:g.193642833C>G	GRCh38
NC_000003.11:g.193360622C>G , CM000665.1:g.193360622C>G	GRCh37
NC_000003.10:g.194843316C>G	NCBI36
NG_011605.1:g.54690C>G , LRG_337:g.54690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1218C>G MANE Select	ENSP00000355324.2:p.Thr406=
ENST00000361828.7:c.1053C>G	ENSP00000354429.3:p.Thr351=
ENST00000361908.8:c.1164C>G	ENSP00000354681.3:p.Thr388=
ENST00000392436.7:c.1053C>G	ENSP00000376231.3:p.Thr351=
ENST00000392437.6:c.1107C>G	ENSP00000376232.2:p.Thr369=
ENST00000642289.1:c.1080-540C>G
ENST00000642445.1:c.1053C>G	ENSP00000495535.1:p.Thr351=
ENST00000642593.1:c.1053C>G	ENSP00000494273.1:p.Thr351=
ENST00000643329.1:c.735C>G	ENSP00000493673.1:p.Thr245=
ENST00000643737.1:c.*1134C>G	ENSP00000494210.1:n.*1134C>G
ENST00000644595.1:c.1053C>G	ENSP00000494121.1:p.Thr351=
ENST00000644629.1:c.713C>G
ENST00000644841.1:c.681C>G	ENSP00000493988.1:p.Thr227=
ENST00000644959.1:c.1022C>G
ENST00000645553.1:c.1068C>G	ENSP00000494725.1:p.Thr356=
ENST00000646085.1:c.*531C>G	ENSP00000494509.1:n.*531C>G
ENST00000646277.1:c.1218C>G	ENSP00000495289.1:p.Thr406=
ENST00000646544.1:c.116C>G
ENST00000646699.1:c.1080-540C>G
ENST00000646793.1:c.945C>G	ENSP00000494512.1:p.Thr315=
ENST00000361150.6:c.1056C>G	ENSP00000354781.2:p.Thr352=
ENST00000361510.6:c.1218C>G	ENSP00000355324.2:p.Thr406=
ENST00000361715.6:c.1110C>G	ENSP00000355311.2:p.Thr370=
ENST00000361828.6:c.1107C>G	ENSP00000354429.2:p.Thr369=
ENST00000361908.7:c.1164C>G	ENSP00000354681.3:p.Thr388=
ENST00000392438.7:c.1053C>G	ENSP00000376233.3:p.Thr351=
ENST00000475899.1:n.249C>G
ENST00000497189.5:n.539C>G
NM_015560.2:c.1053C>G , LRG_337t1:c.1053C>G	NP_056375.2:p.Thr351=
NM_130831.2:c.945C>G	NP_570844.1:p.Thr315=
NM_130832.2:c.999C>G	NP_570845.1:p.Thr333=
NM_130833.2:c.1056C>G	NP_570846.1:p.Thr352=
NM_130834.2:c.1107C>G	NP_570847.2:p.Thr369=
NM_130835.2:c.1110C>G	NP_570848.1:p.Thr370=
NM_130836.2:c.1164C>G	NP_570849.2:p.Thr388=
NM_130837.2:c.1218C>G , LRG_337t2:c.1218C>G	NP_570850.2:p.Thr406=
XM_011512863.1:c.1218C>G	XP_011511165.1:p.Thr406=
XM_011512864.1:c.1164C>G	XP_011511166.1:p.Thr388=
XM_011512865.1:c.1107C>G	XP_011511167.1:p.Thr369=
XM_011512866.1:c.1056C>G	XP_011511168.1:p.Thr352=
XM_011512867.1:c.1053C>G	XP_011511169.1:p.Thr351=
XM_011512868.1:c.945C>G	XP_011511170.1:p.Thr315=
XM_011512869.1:c.1218C>G	XP_011511171.1:p.Thr406=
NM_001354663.1:c.684C>G	NP_001341592.1:p.Thr228=
NM_001354664.1:c.681C>G	NP_001341593.1:p.Thr227=
XR_001740158.2:n.1447C>G
XR_001740159.2:n.1282C>G
NM_001354663.2:c.684C>G	NP_001341592.1:p.Thr228=
NM_001354664.2:c.681C>G	NP_001341593.1:p.Thr227=
NM_130831.3:c.945C>G	NP_570844.1:p.Thr315=
NM_130832.3:c.999C>G	NP_570845.1:p.Thr333=
NM_130834.3:c.1107C>G	NP_570847.2:p.Thr369=
NM_130836.3:c.1164C>G	NP_570849.2:p.Thr388=
NM_015560.3:c.1053C>G	NP_056375.2:p.Thr351=
NM_130833.3:c.1056C>G	NP_570846.1:p.Thr352=
NM_130835.3:c.1110C>G	NP_570848.1:p.Thr370=
NM_130837.3:c.1218C>G MANE Select	NP_570850.2:p.Thr406=