Canonical Allele Identifier: CA437437534

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193364920T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647131T>C , CM000665.2:g.193647131T>C	GRCh38
NC_000003.11:g.193364920T>C , CM000665.1:g.193364920T>C	GRCh37
NC_000003.10:g.194847614T>C	NCBI36
NG_011605.1:g.58988T>C , LRG_337:g.58988T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1821T>C MANE Select	ENSP00000355324.2:p.Phe607=
ENST00000361828.7:c.1656T>C	ENSP00000354429.3:p.Phe552=
ENST00000361908.8:c.1767T>C	ENSP00000354681.3:p.Phe589=
ENST00000392436.7:c.1656T>C	ENSP00000376231.3:p.Phe552=
ENST00000392437.6:c.1710T>C	ENSP00000376232.2:p.Phe570=
ENST00000642289.1:c.1595T>C
ENST00000642445.1:c.1656T>C	ENSP00000495535.1:p.Phe552=
ENST00000642593.1:c.1656T>C	ENSP00000494273.1:p.Phe552=
ENST00000643329.1:c.1338T>C	ENSP00000493673.1:p.Phe446=
ENST00000643737.1:c.*1737T>C	ENSP00000494210.1:n.*1737T>C
ENST00000644595.1:c.1656T>C	ENSP00000494121.1:p.Phe552=
ENST00000644629.1:c.1243T>C
ENST00000644841.1:c.*140T>C	ENSP00000493988.1:n.*140T>C
ENST00000644959.1:c.1625T>C
ENST00000645553.1:c.1671T>C	ENSP00000494725.1:p.Phe557=
ENST00000646085.1:c.*1134T>C	ENSP00000494509.1:n.*1134T>C
ENST00000646277.1:c.*257T>C	ENSP00000495289.1:n.*257T>C
ENST00000646544.1:c.644T>C
ENST00000646699.1:c.1595T>C
ENST00000646793.1:c.1548T>C	ENSP00000494512.1:p.Phe516=
ENST00000361150.6:c.1659T>C	ENSP00000354781.2:p.Phe553=
ENST00000361510.6:c.1821T>C	ENSP00000355324.2:p.Phe607=
ENST00000361715.6:c.1713T>C	ENSP00000355311.2:p.Phe571=
ENST00000361828.6:c.1710T>C	ENSP00000354429.2:p.Phe570=
ENST00000361908.7:c.1767T>C	ENSP00000354681.3:p.Phe589=
ENST00000392438.7:c.1656T>C	ENSP00000376233.3:p.Phe552=
ENST00000483516.1:n.154T>C
NM_015560.2:c.1656T>C , LRG_337t1:c.1656T>C	NP_056375.2:p.Phe552=
NM_130831.2:c.1548T>C	NP_570844.1:p.Phe516=
NM_130832.2:c.1602T>C	NP_570845.1:p.Phe534=
NM_130833.2:c.1659T>C	NP_570846.1:p.Phe553=
NM_130834.2:c.1710T>C	NP_570847.2:p.Phe570=
NM_130835.2:c.1713T>C	NP_570848.1:p.Phe571=
NM_130836.2:c.1767T>C	NP_570849.2:p.Phe589=
NM_130837.2:c.1821T>C , LRG_337t2:c.1821T>C	NP_570850.2:p.Phe607=
XM_011512863.1:c.1821T>C	XP_011511165.1:p.Phe607=
XM_011512864.1:c.1767T>C	XP_011511166.1:p.Phe589=
XM_011512865.1:c.1710T>C	XP_011511167.1:p.Phe570=
XM_011512866.1:c.1659T>C	XP_011511168.1:p.Phe553=
XM_011512867.1:c.1656T>C	XP_011511169.1:p.Phe552=
XM_011512868.1:c.1548T>C	XP_011511170.1:p.Phe516=
XM_011512869.1:c.1821T>C	XP_011511171.1:p.Phe607=
NM_001354663.1:c.1287T>C	NP_001341592.1:p.Phe429=
NM_001354664.1:c.1284T>C	NP_001341593.1:p.Phe428=
XR_001740158.2:n.2050T>C
XR_001740159.2:n.1885T>C
NM_001354663.2:c.1287T>C	NP_001341592.1:p.Phe429=
NM_001354664.2:c.1284T>C	NP_001341593.1:p.Phe428=
NM_130831.3:c.1548T>C	NP_570844.1:p.Phe516=
NM_130832.3:c.1602T>C	NP_570845.1:p.Phe534=
NM_130834.3:c.1710T>C	NP_570847.2:p.Phe570=
NM_130836.3:c.1767T>C	NP_570849.2:p.Phe589=
NM_015560.3:c.1656T>C	NP_056375.2:p.Phe552=
NM_130833.3:c.1659T>C	NP_570846.1:p.Phe553=
NM_130835.3:c.1713T>C	NP_570848.1:p.Phe571=
NM_130837.3:c.1821T>C MANE Select	NP_570850.2:p.Phe607=