Canonical Allele Identifier: CA355793305

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193380740G>T (hg19) ; chr3:g.193662951G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662951G>T , CM000665.2:g.193662951G>T	GRCh38
NC_000003.11:g.193380740G>T , CM000665.1:g.193380740G>T	GRCh37
NC_000003.10:g.194863434G>T	NCBI36
NG_011605.1:g.74808G>T , LRG_337:g.74808G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2650G>T MANE Select	ENSP00000355324.2:p.Asp884Tyr
ENST00000361828.7:c.2485G>T	ENSP00000354429.3:p.Asp829Tyr
ENST00000361908.8:c.2596G>T	ENSP00000354681.3:p.Asp866Tyr
ENST00000392436.7:c.2485G>T	ENSP00000376231.3:p.Asp829Tyr
ENST00000392437.6:c.2539G>T	ENSP00000376232.2:p.Asp847Tyr
ENST00000642289.1:c.2424G>T
ENST00000642445.1:c.2485G>T	ENSP00000495535.1:p.Asp829Tyr
ENST00000642593.1:c.*710G>T	ENSP00000494273.1:n.*710G>T
ENST00000643329.1:c.2167G>T	ENSP00000493673.1:p.Asp723Tyr
ENST00000643737.1:c.*2566G>T	ENSP00000494210.1:n.*2566G>T
ENST00000644595.1:c.2485G>T	ENSP00000494121.1:p.Asp829Tyr
ENST00000644629.1:c.2072G>T
ENST00000644841.1:c.*969G>T	ENSP00000493988.1:n.*969G>T
ENST00000644959.1:c.2479G>T
ENST00000645553.1:c.2500G>T	ENSP00000494725.1:p.Asp834Tyr
ENST00000646085.1:c.*1963G>T	ENSP00000494509.1:n.*1963G>T
ENST00000646277.1:c.*1086G>T	ENSP00000495289.1:n.*1086G>T
ENST00000646544.1:c.1473G>T
ENST00000646699.1:c.2424G>T
ENST00000646793.1:c.2377G>T	ENSP00000494512.1:p.Asp793Tyr
ENST00000361150.6:c.2488G>T	ENSP00000354781.2:p.Asp830Tyr
ENST00000361510.6:c.2650G>T	ENSP00000355324.2:p.Asp884Tyr
ENST00000361715.6:c.2542G>T	ENSP00000355311.2:p.Asp848Tyr
ENST00000361828.6:c.2539G>T	ENSP00000354429.2:p.Asp847Tyr
ENST00000361908.7:c.2596G>T	ENSP00000354681.3:p.Asp866Tyr
ENST00000392438.7:c.2485G>T	ENSP00000376233.3:p.Asp829Tyr
ENST00000445863.1:c.61G>T	ENSP00000398358.1:p.Asp21Tyr
NM_015560.2:c.2485G>T , LRG_337t1:c.2485G>T	NP_056375.2:p.Asp829Tyr
NM_130831.2:c.2377G>T	NP_570844.1:p.Asp793Tyr
NM_130832.2:c.2431G>T	NP_570845.1:p.Asp811Tyr
NM_130833.2:c.2488G>T	NP_570846.1:p.Asp830Tyr
NM_130834.2:c.2539G>T	NP_570847.2:p.Asp847Tyr
NM_130835.2:c.2542G>T	NP_570848.1:p.Asp848Tyr
NM_130836.2:c.2596G>T	NP_570849.2:p.Asp866Tyr
NM_130837.2:c.2650G>T , LRG_337t2:c.2650G>T	NP_570850.2:p.Asp884Tyr
XM_011512863.1:c.2650G>T	XP_011511165.1:p.Asp884Tyr
XM_011512864.1:c.2596G>T	XP_011511166.1:p.Asp866Tyr
XM_011512865.1:c.2539G>T	XP_011511167.1:p.Asp847Tyr
XM_011512866.1:c.2488G>T	XP_011511168.1:p.Asp830Tyr
XM_011512867.1:c.2485G>T	XP_011511169.1:p.Asp829Tyr
XM_011512868.1:c.2377G>T	XP_011511170.1:p.Asp793Tyr
XR_924835.1:n.582+5969C>A
NM_001354663.1:c.2116G>T	NP_001341592.1:p.Asp706Tyr
NM_001354664.1:c.2113G>T	NP_001341593.1:p.Asp705Tyr
XR_001740158.2:n.2904G>T
XR_001740159.2:n.2739G>T
XR_001741072.1:n.601-2866C>A
XR_001741074.1:n.475+7857C>A
XR_924835.2:n.600+5969C>A
NM_001354663.2:c.2116G>T	NP_001341592.1:p.Asp706Tyr
NM_001354664.2:c.2113G>T	NP_001341593.1:p.Asp705Tyr
NM_130831.3:c.2377G>T	NP_570844.1:p.Asp793Tyr
NM_130832.3:c.2431G>T	NP_570845.1:p.Asp811Tyr
NM_130834.3:c.2539G>T	NP_570847.2:p.Asp847Tyr
NM_130836.3:c.2596G>T	NP_570849.2:p.Asp866Tyr
NM_015560.3:c.2485G>T	NP_056375.2:p.Asp829Tyr
NM_130833.3:c.2488G>T	NP_570846.1:p.Asp830Tyr
NM_130835.3:c.2542G>T	NP_570848.1:p.Asp848Tyr
NM_130837.3:c.2650G>T MANE Select	NP_570850.2:p.Asp884Tyr