Canonical Allele Identifier: CA437434487

Gene: OPA1

Linked Data

• gnomAD v4: 3-193638029-A-G
• MyVariant Identifiers: chr3:g.193355818A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193638029A>G , CM000665.2:g.193638029A>G	GRCh38
NC_000003.11:g.193355818A>G , CM000665.1:g.193355818A>G	GRCh37
NC_000003.10:g.194838512A>G	NCBI36
NG_011605.1:g.49886A>G , LRG_337:g.49886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1113A>G MANE Select	ENSP00000355324.2:p.Arg371=
ENST00000361828.7:c.948A>G	ENSP00000354429.3:p.Arg316=
ENST00000361908.8:c.1059A>G	ENSP00000354681.3:p.Arg353=
ENST00000392436.7:c.948A>G	ENSP00000376231.3:p.Arg316=
ENST00000392437.6:c.1002A>G	ENSP00000376232.2:p.Arg334=
ENST00000642289.1:c.1043A>G
ENST00000642445.1:c.948A>G	ENSP00000495535.1:p.Arg316=
ENST00000642593.1:c.948A>G	ENSP00000494273.1:p.Arg316=
ENST00000643329.1:c.630A>G	ENSP00000493673.1:p.Arg210=
ENST00000643737.1:c.*1029A>G	ENSP00000494210.1:n.*1029A>G
ENST00000644595.1:c.948A>G	ENSP00000494121.1:p.Arg316=
ENST00000644629.1:c.608A>G
ENST00000644841.1:c.576A>G	ENSP00000493988.1:p.Arg192=
ENST00000644959.1:c.917A>G
ENST00000645553.1:c.963A>G	ENSP00000494725.1:p.Arg321=
ENST00000646085.1:c.*426A>G	ENSP00000494509.1:n.*426A>G
ENST00000646277.1:c.1113A>G	ENSP00000495289.1:p.Arg371=
ENST00000646544.1:c.11A>G
ENST00000646699.1:c.1043A>G
ENST00000646793.1:c.840A>G	ENSP00000494512.1:p.Arg280=
ENST00000361150.6:c.951A>G	ENSP00000354781.2:p.Arg317=
ENST00000361510.6:c.1113A>G	ENSP00000355324.2:p.Arg371=
ENST00000361715.6:c.1005A>G	ENSP00000355311.2:p.Arg335=
ENST00000361828.6:c.1002A>G	ENSP00000354429.2:p.Arg334=
ENST00000361908.7:c.1059A>G	ENSP00000354681.3:p.Arg353=
ENST00000392438.7:c.948A>G	ENSP00000376233.3:p.Arg316=
ENST00000475899.1:n.144A>G
ENST00000495476.1:n.469A>G
ENST00000497189.5:n.434A>G
NM_015560.2:c.948A>G , LRG_337t1:c.948A>G	NP_056375.2:p.Arg316=
NM_130831.2:c.840A>G	NP_570844.1:p.Arg280=
NM_130832.2:c.894A>G	NP_570845.1:p.Arg298=
NM_130833.2:c.951A>G	NP_570846.1:p.Arg317=
NM_130834.2:c.1002A>G	NP_570847.2:p.Arg334=
NM_130835.2:c.1005A>G	NP_570848.1:p.Arg335=
NM_130836.2:c.1059A>G	NP_570849.2:p.Arg353=
NM_130837.2:c.1113A>G , LRG_337t2:c.1113A>G	NP_570850.2:p.Arg371=
XM_011512863.1:c.1113A>G	XP_011511165.1:p.Arg371=
XM_011512864.1:c.1059A>G	XP_011511166.1:p.Arg353=
XM_011512865.1:c.1002A>G	XP_011511167.1:p.Arg334=
XM_011512866.1:c.951A>G	XP_011511168.1:p.Arg317=
XM_011512867.1:c.948A>G	XP_011511169.1:p.Arg316=
XM_011512868.1:c.840A>G	XP_011511170.1:p.Arg280=
XM_011512869.1:c.1113A>G	XP_011511171.1:p.Arg371=
NM_001354663.1:c.579A>G	NP_001341592.1:p.Arg193=
NM_001354664.1:c.576A>G	NP_001341593.1:p.Arg192=
XR_001740158.2:n.1342A>G
XR_001740159.2:n.1177A>G
NM_001354663.2:c.579A>G	NP_001341592.1:p.Arg193=
NM_001354664.2:c.576A>G	NP_001341593.1:p.Arg192=
NM_130831.3:c.840A>G	NP_570844.1:p.Arg280=
NM_130832.3:c.894A>G	NP_570845.1:p.Arg298=
NM_130834.3:c.1002A>G	NP_570847.2:p.Arg334=
NM_130836.3:c.1059A>G	NP_570849.2:p.Arg353=
NM_015560.3:c.948A>G	NP_056375.2:p.Arg316=
NM_130833.3:c.951A>G	NP_570846.1:p.Arg317=
NM_130835.3:c.1005A>G	NP_570848.1:p.Arg335=
NM_130837.3:c.1113A>G MANE Select	NP_570850.2:p.Arg371=