Canonical Allele Identifier: CA437441599

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193380685A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662896A>T , CM000665.2:g.193662896A>T	GRCh38
NC_000003.11:g.193380685A>T , CM000665.1:g.193380685A>T	GRCh37
NC_000003.10:g.194863379A>T	NCBI36
NG_011605.1:g.74753A>T , LRG_337:g.74753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2595A>T MANE Select	ENSP00000355324.2:p.Ala865=
ENST00000361828.7:c.2430A>T	ENSP00000354429.3:p.Ala810=
ENST00000361908.8:c.2541A>T	ENSP00000354681.3:p.Ala847=
ENST00000392436.7:c.2430A>T	ENSP00000376231.3:p.Ala810=
ENST00000392437.6:c.2484A>T	ENSP00000376232.2:p.Ala828=
ENST00000642289.1:c.2369A>T
ENST00000642445.1:c.2430A>T	ENSP00000495535.1:p.Ala810=
ENST00000642593.1:c.*655A>T	ENSP00000494273.1:n.*655A>T
ENST00000643329.1:c.2112A>T	ENSP00000493673.1:p.Ala704=
ENST00000643737.1:c.*2511A>T	ENSP00000494210.1:n.*2511A>T
ENST00000644595.1:c.2430A>T	ENSP00000494121.1:p.Ala810=
ENST00000644629.1:c.2017A>T
ENST00000644841.1:c.*914A>T	ENSP00000493988.1:n.*914A>T
ENST00000644959.1:c.2424A>T
ENST00000645553.1:c.2445A>T	ENSP00000494725.1:p.Ala815=
ENST00000646085.1:c.*1908A>T	ENSP00000494509.1:n.*1908A>T
ENST00000646277.1:c.*1031A>T	ENSP00000495289.1:n.*1031A>T
ENST00000646544.1:c.1418A>T
ENST00000646699.1:c.2369A>T
ENST00000646793.1:c.2322A>T	ENSP00000494512.1:p.Ala774=
ENST00000361150.6:c.2433A>T	ENSP00000354781.2:p.Ala811=
ENST00000361510.6:c.2595A>T	ENSP00000355324.2:p.Ala865=
ENST00000361715.6:c.2487A>T	ENSP00000355311.2:p.Ala829=
ENST00000361828.6:c.2484A>T	ENSP00000354429.2:p.Ala828=
ENST00000361908.7:c.2541A>T	ENSP00000354681.3:p.Ala847=
ENST00000392438.7:c.2430A>T	ENSP00000376233.3:p.Ala810=
ENST00000445863.1:c.6A>T	ENSP00000398358.1:p.Ala2=
NM_015560.2:c.2430A>T , LRG_337t1:c.2430A>T	NP_056375.2:p.Ala810=
NM_130831.2:c.2322A>T	NP_570844.1:p.Ala774=
NM_130832.2:c.2376A>T	NP_570845.1:p.Ala792=
NM_130833.2:c.2433A>T	NP_570846.1:p.Ala811=
NM_130834.2:c.2484A>T	NP_570847.2:p.Ala828=
NM_130835.2:c.2487A>T	NP_570848.1:p.Ala829=
NM_130836.2:c.2541A>T	NP_570849.2:p.Ala847=
NM_130837.2:c.2595A>T , LRG_337t2:c.2595A>T	NP_570850.2:p.Ala865=
XM_011512863.1:c.2595A>T	XP_011511165.1:p.Ala865=
XM_011512864.1:c.2541A>T	XP_011511166.1:p.Ala847=
XM_011512865.1:c.2484A>T	XP_011511167.1:p.Ala828=
XM_011512866.1:c.2433A>T	XP_011511168.1:p.Ala811=
XM_011512867.1:c.2430A>T	XP_011511169.1:p.Ala810=
XM_011512868.1:c.2322A>T	XP_011511170.1:p.Ala774=
XR_924835.1:n.582+6024T>A
NM_001354663.1:c.2061A>T	NP_001341592.1:p.Ala687=
NM_001354664.1:c.2058A>T	NP_001341593.1:p.Ala686=
XR_001740158.2:n.2849A>T
XR_001740159.2:n.2684A>T
XR_001741072.1:n.601-2811T>A
XR_001741074.1:n.475+7912T>A
XR_924835.2:n.600+6024T>A
NM_001354663.2:c.2061A>T	NP_001341592.1:p.Ala687=
NM_001354664.2:c.2058A>T	NP_001341593.1:p.Ala686=
NM_130831.3:c.2322A>T	NP_570844.1:p.Ala774=
NM_130832.3:c.2376A>T	NP_570845.1:p.Ala792=
NM_130834.3:c.2484A>T	NP_570847.2:p.Ala828=
NM_130836.3:c.2541A>T	NP_570849.2:p.Ala847=
NM_015560.3:c.2430A>T	NP_056375.2:p.Ala810=
NM_130833.3:c.2433A>T	NP_570846.1:p.Ala811=
NM_130835.3:c.2487A>T	NP_570848.1:p.Ala829=
NM_130837.3:c.2595A>T MANE Select	NP_570850.2:p.Ala865=