Canonical Allele Identifier: CA355792806

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377276A>G (hg19) ; chr3:g.193659487A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659487A>G , CM000665.2:g.193659487A>G	GRCh38
NC_000003.11:g.193377276A>G , CM000665.1:g.193377276A>G	GRCh37
NC_000003.10:g.194859970A>G	NCBI36
NG_011605.1:g.71344A>G , LRG_337:g.71344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2446A>G MANE Select	ENSP00000355324.2:p.Asn816Asp
ENST00000361828.7:c.2281A>G	ENSP00000354429.3:p.Asn761Asp
ENST00000361908.8:c.2392A>G	ENSP00000354681.3:p.Asn798Asp
ENST00000392436.7:c.2281A>G	ENSP00000376231.3:p.Asn761Asp
ENST00000392437.6:c.2335A>G	ENSP00000376232.2:p.Asn779Asp
ENST00000642289.1:c.2220A>G
ENST00000642445.1:c.2281A>G	ENSP00000495535.1:p.Asn761Asp
ENST00000642593.1:c.*506A>G	ENSP00000494273.1:n.*506A>G
ENST00000643329.1:c.1963A>G	ENSP00000493673.1:p.Asn655Asp
ENST00000643737.1:c.*2362A>G	ENSP00000494210.1:n.*2362A>G
ENST00000644595.1:c.2281A>G	ENSP00000494121.1:p.Asn761Asp
ENST00000644629.1:c.1868A>G
ENST00000644841.1:c.*765A>G	ENSP00000493988.1:n.*765A>G
ENST00000644959.1:c.2275A>G
ENST00000645553.1:c.2296A>G	ENSP00000494725.1:p.Asn766Asp
ENST00000646085.1:c.*1759A>G	ENSP00000494509.1:n.*1759A>G
ENST00000646277.1:c.*882A>G	ENSP00000495289.1:n.*882A>G
ENST00000646544.1:c.1269A>G
ENST00000646699.1:c.2220A>G
ENST00000646793.1:c.2173A>G	ENSP00000494512.1:p.Asn725Asp
ENST00000361150.6:c.2284A>G	ENSP00000354781.2:p.Asn762Asp
ENST00000361510.6:c.2446A>G	ENSP00000355324.2:p.Asn816Asp
ENST00000361715.6:c.2338A>G	ENSP00000355311.2:p.Asn780Asp
ENST00000361828.6:c.2335A>G	ENSP00000354429.2:p.Asn779Asp
ENST00000361908.7:c.2392A>G	ENSP00000354681.3:p.Asn798Asp
ENST00000392438.7:c.2281A>G	ENSP00000376233.3:p.Asn761Asp
ENST00000482865.1:n.540A>G
NM_015560.2:c.2281A>G , LRG_337t1:c.2281A>G	NP_056375.2:p.Asn761Asp
NM_130831.2:c.2173A>G	NP_570844.1:p.Asn725Asp
NM_130832.2:c.2227A>G	NP_570845.1:p.Asn743Asp
NM_130833.2:c.2284A>G	NP_570846.1:p.Asn762Asp
NM_130834.2:c.2335A>G	NP_570847.2:p.Asn779Asp
NM_130835.2:c.2338A>G	NP_570848.1:p.Asn780Asp
NM_130836.2:c.2392A>G	NP_570849.2:p.Asn798Asp
NM_130837.2:c.2446A>G , LRG_337t2:c.2446A>G	NP_570850.2:p.Asn816Asp
XM_011512863.1:c.2446A>G	XP_011511165.1:p.Asn816Asp
XM_011512864.1:c.2392A>G	XP_011511166.1:p.Asn798Asp
XM_011512865.1:c.2335A>G	XP_011511167.1:p.Asn779Asp
XM_011512866.1:c.2284A>G	XP_011511168.1:p.Asn762Asp
XM_011512867.1:c.2281A>G	XP_011511169.1:p.Asn761Asp
XM_011512868.1:c.2173A>G	XP_011511170.1:p.Asn725Asp
XR_924835.1:n.582+9433T>C
NM_001354663.1:c.1912A>G	NP_001341592.1:p.Asn638Asp
NM_001354664.1:c.1909A>G	NP_001341593.1:p.Asn637Asp
XR_001740158.2:n.2700A>G
XR_001740159.2:n.2535A>G
XR_001741074.1:n.475+11321T>C
XR_924835.2:n.600+9433T>C
NM_001354663.2:c.1912A>G	NP_001341592.1:p.Asn638Asp
NM_001354664.2:c.1909A>G	NP_001341593.1:p.Asn637Asp
NM_130831.3:c.2173A>G	NP_570844.1:p.Asn725Asp
NM_130832.3:c.2227A>G	NP_570845.1:p.Asn743Asp
NM_130834.3:c.2335A>G	NP_570847.2:p.Asn779Asp
NM_130836.3:c.2392A>G	NP_570849.2:p.Asn798Asp
NM_015560.3:c.2281A>G	NP_056375.2:p.Asn761Asp
NM_130833.3:c.2284A>G	NP_570846.1:p.Asn762Asp
NM_130835.3:c.2338A>G	NP_570848.1:p.Asn780Asp
NM_130837.3:c.2446A>G MANE Select	NP_570850.2:p.Asn816Asp