Canonical Allele Identifier: CA355793241

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193380714A>T (hg19) ; chr3:g.193662925A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662925A>T , CM000665.2:g.193662925A>T	GRCh38
NC_000003.11:g.193380714A>T , CM000665.1:g.193380714A>T	GRCh37
NC_000003.10:g.194863408A>T	NCBI36
NG_011605.1:g.74782A>T , LRG_337:g.74782A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2624A>T MANE Select	ENSP00000355324.2:p.Asn875Ile
ENST00000361828.7:c.2459A>T	ENSP00000354429.3:p.Asn820Ile
ENST00000361908.8:c.2570A>T	ENSP00000354681.3:p.Asn857Ile
ENST00000392436.7:c.2459A>T	ENSP00000376231.3:p.Asn820Ile
ENST00000392437.6:c.2513A>T	ENSP00000376232.2:p.Asn838Ile
ENST00000642289.1:c.2398A>T
ENST00000642445.1:c.2459A>T	ENSP00000495535.1:p.Asn820Ile
ENST00000642593.1:c.*684A>T	ENSP00000494273.1:n.*684A>T
ENST00000643329.1:c.2141A>T	ENSP00000493673.1:p.Asn714Ile
ENST00000643737.1:c.*2540A>T	ENSP00000494210.1:n.*2540A>T
ENST00000644595.1:c.2459A>T	ENSP00000494121.1:p.Asn820Ile
ENST00000644629.1:c.2046A>T
ENST00000644841.1:c.*943A>T	ENSP00000493988.1:n.*943A>T
ENST00000644959.1:c.2453A>T
ENST00000645553.1:c.2474A>T	ENSP00000494725.1:p.Asn825Ile
ENST00000646085.1:c.*1937A>T	ENSP00000494509.1:n.*1937A>T
ENST00000646277.1:c.*1060A>T	ENSP00000495289.1:n.*1060A>T
ENST00000646544.1:c.1447A>T
ENST00000646699.1:c.2398A>T
ENST00000646793.1:c.2351A>T	ENSP00000494512.1:p.Asn784Ile
ENST00000361150.6:c.2462A>T	ENSP00000354781.2:p.Asn821Ile
ENST00000361510.6:c.2624A>T	ENSP00000355324.2:p.Asn875Ile
ENST00000361715.6:c.2516A>T	ENSP00000355311.2:p.Asn839Ile
ENST00000361828.6:c.2513A>T	ENSP00000354429.2:p.Asn838Ile
ENST00000361908.7:c.2570A>T	ENSP00000354681.3:p.Asn857Ile
ENST00000392438.7:c.2459A>T	ENSP00000376233.3:p.Asn820Ile
ENST00000445863.1:c.35A>T	ENSP00000398358.1:p.Asn12Ile
NM_015560.2:c.2459A>T , LRG_337t1:c.2459A>T	NP_056375.2:p.Asn820Ile
NM_130831.2:c.2351A>T	NP_570844.1:p.Asn784Ile
NM_130832.2:c.2405A>T	NP_570845.1:p.Asn802Ile
NM_130833.2:c.2462A>T	NP_570846.1:p.Asn821Ile
NM_130834.2:c.2513A>T	NP_570847.2:p.Asn838Ile
NM_130835.2:c.2516A>T	NP_570848.1:p.Asn839Ile
NM_130836.2:c.2570A>T	NP_570849.2:p.Asn857Ile
NM_130837.2:c.2624A>T , LRG_337t2:c.2624A>T	NP_570850.2:p.Asn875Ile
XM_011512863.1:c.2624A>T	XP_011511165.1:p.Asn875Ile
XM_011512864.1:c.2570A>T	XP_011511166.1:p.Asn857Ile
XM_011512865.1:c.2513A>T	XP_011511167.1:p.Asn838Ile
XM_011512866.1:c.2462A>T	XP_011511168.1:p.Asn821Ile
XM_011512867.1:c.2459A>T	XP_011511169.1:p.Asn820Ile
XM_011512868.1:c.2351A>T	XP_011511170.1:p.Asn784Ile
XR_924835.1:n.582+5995T>A
NM_001354663.1:c.2090A>T	NP_001341592.1:p.Asn697Ile
NM_001354664.1:c.2087A>T	NP_001341593.1:p.Asn696Ile
XR_001740158.2:n.2878A>T
XR_001740159.2:n.2713A>T
XR_001741072.1:n.601-2840T>A
XR_001741074.1:n.475+7883T>A
XR_924835.2:n.600+5995T>A
NM_001354663.2:c.2090A>T	NP_001341592.1:p.Asn697Ile
NM_001354664.2:c.2087A>T	NP_001341593.1:p.Asn696Ile
NM_130831.3:c.2351A>T	NP_570844.1:p.Asn784Ile
NM_130832.3:c.2405A>T	NP_570845.1:p.Asn802Ile
NM_130834.3:c.2513A>T	NP_570847.2:p.Asn838Ile
NM_130836.3:c.2570A>T	NP_570849.2:p.Asn857Ile
NM_015560.3:c.2459A>T	NP_056375.2:p.Asn820Ile
NM_130833.3:c.2462A>T	NP_570846.1:p.Asn821Ile
NM_130835.3:c.2516A>T	NP_570848.1:p.Asn839Ile
NM_130837.3:c.2624A>T MANE Select	NP_570850.2:p.Asn875Ile