Canonical Allele Identifier: CA437436062

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193361319T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643530T>G , CM000665.2:g.193643530T>G	GRCh38
NC_000003.11:g.193361319T>G , CM000665.1:g.193361319T>G	GRCh37
NC_000003.10:g.194844013T>G	NCBI36
NG_011605.1:g.55387T>G , LRG_337:g.55387T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1380T>G MANE Select	ENSP00000355324.2:p.Thr460=
ENST00000361828.7:c.1215T>G	ENSP00000354429.3:p.Thr405=
ENST00000361908.8:c.1326T>G	ENSP00000354681.3:p.Thr442=
ENST00000392436.7:c.1215T>G	ENSP00000376231.3:p.Thr405=
ENST00000392437.6:c.1269T>G	ENSP00000376232.2:p.Thr423=
ENST00000642289.1:c.1154T>G
ENST00000642445.1:c.1215T>G	ENSP00000495535.1:p.Thr405=
ENST00000642593.1:c.1215T>G	ENSP00000494273.1:p.Thr405=
ENST00000643329.1:c.897T>G	ENSP00000493673.1:p.Thr299=
ENST00000643737.1:c.*1296T>G	ENSP00000494210.1:n.*1296T>G
ENST00000644595.1:c.1215T>G	ENSP00000494121.1:p.Thr405=
ENST00000644629.1:c.875T>G
ENST00000644841.1:c.843T>G	ENSP00000493988.1:p.Thr281=
ENST00000644959.1:c.1184T>G
ENST00000645553.1:c.1230T>G	ENSP00000494725.1:p.Thr410=
ENST00000646085.1:c.*693T>G	ENSP00000494509.1:n.*693T>G
ENST00000646277.1:c.1380T>G	ENSP00000495289.1:p.Thr460=
ENST00000646544.1:c.203T>G
ENST00000646699.1:c.1154T>G
ENST00000646793.1:c.1107T>G	ENSP00000494512.1:p.Thr369=
ENST00000361150.6:c.1218T>G	ENSP00000354781.2:p.Thr406=
ENST00000361510.6:c.1380T>G	ENSP00000355324.2:p.Thr460=
ENST00000361715.6:c.1272T>G	ENSP00000355311.2:p.Thr424=
ENST00000361828.6:c.1269T>G	ENSP00000354429.2:p.Thr423=
ENST00000361908.7:c.1326T>G	ENSP00000354681.3:p.Thr442=
ENST00000392438.7:c.1215T>G	ENSP00000376233.3:p.Thr405=
ENST00000475899.1:n.411T>G
NM_015560.2:c.1215T>G , LRG_337t1:c.1215T>G	NP_056375.2:p.Thr405=
NM_130831.2:c.1107T>G	NP_570844.1:p.Thr369=
NM_130832.2:c.1161T>G	NP_570845.1:p.Thr387=
NM_130833.2:c.1218T>G	NP_570846.1:p.Thr406=
NM_130834.2:c.1269T>G	NP_570847.2:p.Thr423=
NM_130835.2:c.1272T>G	NP_570848.1:p.Thr424=
NM_130836.2:c.1326T>G	NP_570849.2:p.Thr442=
NM_130837.2:c.1380T>G , LRG_337t2:c.1380T>G	NP_570850.2:p.Thr460=
XM_011512863.1:c.1380T>G	XP_011511165.1:p.Thr460=
XM_011512864.1:c.1326T>G	XP_011511166.1:p.Thr442=
XM_011512865.1:c.1269T>G	XP_011511167.1:p.Thr423=
XM_011512866.1:c.1218T>G	XP_011511168.1:p.Thr406=
XM_011512867.1:c.1215T>G	XP_011511169.1:p.Thr405=
XM_011512868.1:c.1107T>G	XP_011511170.1:p.Thr369=
XM_011512869.1:c.1380T>G	XP_011511171.1:p.Thr460=
NM_001354663.1:c.846T>G	NP_001341592.1:p.Thr282=
NM_001354664.1:c.843T>G	NP_001341593.1:p.Thr281=
XR_001740158.2:n.1609T>G
XR_001740159.2:n.1444T>G
NM_001354663.2:c.846T>G	NP_001341592.1:p.Thr282=
NM_001354664.2:c.843T>G	NP_001341593.1:p.Thr281=
NM_130831.3:c.1107T>G	NP_570844.1:p.Thr369=
NM_130832.3:c.1161T>G	NP_570845.1:p.Thr387=
NM_130834.3:c.1269T>G	NP_570847.2:p.Thr423=
NM_130836.3:c.1326T>G	NP_570849.2:p.Thr442=
NM_015560.3:c.1215T>G	NP_056375.2:p.Thr405=
NM_130833.3:c.1218T>G	NP_570846.1:p.Thr406=
NM_130835.3:c.1272T>G	NP_570848.1:p.Thr424=
NM_130837.3:c.1380T>G MANE Select	NP_570850.2:p.Thr460=