Canonical Allele Identifier: CA437437543

Gene: OPA1

Linked Data

• ClinVar Variation Id: 899711
• ClinVar RCV Id: RCV001144444
• dbSNP Id: rs1734784679
• gnomAD v4: 3-193647149-G-A
• MyVariant Identifiers: chr3:g.193364938G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647149G>A , CM000665.2:g.193647149G>A	GRCh38
NC_000003.11:g.193364938G>A , CM000665.1:g.193364938G>A	GRCh37
NC_000003.10:g.194847632G>A	NCBI36
NG_011605.1:g.59006G>A , LRG_337:g.59006G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1839G>A MANE Select	ENSP00000355324.2:p.Glu613=
ENST00000361828.7:c.1674G>A	ENSP00000354429.3:p.Glu558=
ENST00000361908.8:c.1785G>A	ENSP00000354681.3:p.Glu595=
ENST00000392436.7:c.1674G>A	ENSP00000376231.3:p.Glu558=
ENST00000392437.6:c.1728G>A	ENSP00000376232.2:p.Glu576=
ENST00000642289.1:c.1613G>A
ENST00000642445.1:c.1674G>A	ENSP00000495535.1:p.Glu558=
ENST00000642593.1:c.1674G>A	ENSP00000494273.1:p.Glu558=
ENST00000643329.1:c.1356G>A	ENSP00000493673.1:p.Glu452=
ENST00000643737.1:c.*1755G>A	ENSP00000494210.1:n.*1755G>A
ENST00000644595.1:c.1674G>A	ENSP00000494121.1:p.Glu558=
ENST00000644629.1:c.1261G>A
ENST00000644841.1:c.*158G>A	ENSP00000493988.1:n.*158G>A
ENST00000644959.1:c.1643G>A
ENST00000645553.1:c.1689G>A	ENSP00000494725.1:p.Glu563=
ENST00000646085.1:c.*1152G>A	ENSP00000494509.1:n.*1152G>A
ENST00000646277.1:c.*275G>A	ENSP00000495289.1:n.*275G>A
ENST00000646544.1:c.662G>A
ENST00000646699.1:c.1613G>A
ENST00000646793.1:c.1566G>A	ENSP00000494512.1:p.Glu522=
ENST00000361150.6:c.1677G>A	ENSP00000354781.2:p.Glu559=
ENST00000361510.6:c.1839G>A	ENSP00000355324.2:p.Glu613=
ENST00000361715.6:c.1731G>A	ENSP00000355311.2:p.Glu577=
ENST00000361828.6:c.1728G>A	ENSP00000354429.2:p.Glu576=
ENST00000361908.7:c.1785G>A	ENSP00000354681.3:p.Glu595=
ENST00000392438.7:c.1674G>A	ENSP00000376233.3:p.Glu558=
ENST00000483516.1:n.172G>A
NM_015560.2:c.1674G>A , LRG_337t1:c.1674G>A	NP_056375.2:p.Glu558=
NM_130831.2:c.1566G>A	NP_570844.1:p.Glu522=
NM_130832.2:c.1620G>A	NP_570845.1:p.Glu540=
NM_130833.2:c.1677G>A	NP_570846.1:p.Glu559=
NM_130834.2:c.1728G>A	NP_570847.2:p.Glu576=
NM_130835.2:c.1731G>A	NP_570848.1:p.Glu577=
NM_130836.2:c.1785G>A	NP_570849.2:p.Glu595=
NM_130837.2:c.1839G>A , LRG_337t2:c.1839G>A	NP_570850.2:p.Glu613=
XM_011512863.1:c.1839G>A	XP_011511165.1:p.Glu613=
XM_011512864.1:c.1785G>A	XP_011511166.1:p.Glu595=
XM_011512865.1:c.1728G>A	XP_011511167.1:p.Glu576=
XM_011512866.1:c.1677G>A	XP_011511168.1:p.Glu559=
XM_011512867.1:c.1674G>A	XP_011511169.1:p.Glu558=
XM_011512868.1:c.1566G>A	XP_011511170.1:p.Glu522=
XM_011512869.1:c.1839G>A	XP_011511171.1:p.Glu613=
NM_001354663.1:c.1305G>A	NP_001341592.1:p.Glu435=
NM_001354664.1:c.1302G>A	NP_001341593.1:p.Glu434=
XR_001740158.2:n.2068G>A
XR_001740159.2:n.1903G>A
NM_001354663.2:c.1305G>A	NP_001341592.1:p.Glu435=
NM_001354664.2:c.1302G>A	NP_001341593.1:p.Glu434=
NM_130831.3:c.1566G>A	NP_570844.1:p.Glu522=
NM_130832.3:c.1620G>A	NP_570845.1:p.Glu540=
NM_130834.3:c.1728G>A	NP_570847.2:p.Glu576=
NM_130836.3:c.1785G>A	NP_570849.2:p.Glu595=
NM_015560.3:c.1674G>A	NP_056375.2:p.Glu558=
NM_130833.3:c.1677G>A	NP_570846.1:p.Glu559=
NM_130835.3:c.1731G>A	NP_570848.1:p.Glu577=
NM_130837.3:c.1839G>A MANE Select	NP_570850.2:p.Glu613=