Canonical Allele Identifier: CA355792972

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377346A>C (hg19) ; chr3:g.193659557A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659557A>C , CM000665.2:g.193659557A>C	GRCh38
NC_000003.11:g.193377346A>C , CM000665.1:g.193377346A>C	GRCh37
NC_000003.10:g.194860040A>C	NCBI36
NG_011605.1:g.71414A>C , LRG_337:g.71414A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2516A>C MANE Select	ENSP00000355324.2:p.Glu839Ala
ENST00000361828.7:c.2351A>C	ENSP00000354429.3:p.Glu784Ala
ENST00000361908.8:c.2462A>C	ENSP00000354681.3:p.Glu821Ala
ENST00000392436.7:c.2351A>C	ENSP00000376231.3:p.Glu784Ala
ENST00000392437.6:c.2405A>C	ENSP00000376232.2:p.Glu802Ala
ENST00000642289.1:c.2290A>C
ENST00000642445.1:c.2351A>C	ENSP00000495535.1:p.Glu784Ala
ENST00000642593.1:c.*576A>C	ENSP00000494273.1:n.*576A>C
ENST00000643329.1:c.2033A>C	ENSP00000493673.1:p.Glu678Ala
ENST00000643737.1:c.*2432A>C	ENSP00000494210.1:n.*2432A>C
ENST00000644595.1:c.2351A>C	ENSP00000494121.1:p.Glu784Ala
ENST00000644629.1:c.1938A>C
ENST00000644841.1:c.*835A>C	ENSP00000493988.1:n.*835A>C
ENST00000644959.1:c.2345A>C
ENST00000645553.1:c.2366A>C	ENSP00000494725.1:p.Glu789Ala
ENST00000646085.1:c.*1829A>C	ENSP00000494509.1:n.*1829A>C
ENST00000646277.1:c.*952A>C	ENSP00000495289.1:n.*952A>C
ENST00000646544.1:c.1339A>C
ENST00000646699.1:c.2290A>C
ENST00000646793.1:c.2243A>C	ENSP00000494512.1:p.Glu748Ala
ENST00000361150.6:c.2354A>C	ENSP00000354781.2:p.Glu785Ala
ENST00000361510.6:c.2516A>C	ENSP00000355324.2:p.Glu839Ala
ENST00000361715.6:c.2408A>C	ENSP00000355311.2:p.Glu803Ala
ENST00000361828.6:c.2405A>C	ENSP00000354429.2:p.Glu802Ala
ENST00000361908.7:c.2462A>C	ENSP00000354681.3:p.Glu821Ala
ENST00000392438.7:c.2351A>C	ENSP00000376233.3:p.Glu784Ala
NM_015560.2:c.2351A>C , LRG_337t1:c.2351A>C	NP_056375.2:p.Glu784Ala
NM_130831.2:c.2243A>C	NP_570844.1:p.Glu748Ala
NM_130832.2:c.2297A>C	NP_570845.1:p.Glu766Ala
NM_130833.2:c.2354A>C	NP_570846.1:p.Glu785Ala
NM_130834.2:c.2405A>C	NP_570847.2:p.Glu802Ala
NM_130835.2:c.2408A>C	NP_570848.1:p.Glu803Ala
NM_130836.2:c.2462A>C	NP_570849.2:p.Glu821Ala
NM_130837.2:c.2516A>C , LRG_337t2:c.2516A>C	NP_570850.2:p.Glu839Ala
XM_011512863.1:c.2516A>C	XP_011511165.1:p.Glu839Ala
XM_011512864.1:c.2462A>C	XP_011511166.1:p.Glu821Ala
XM_011512865.1:c.2405A>C	XP_011511167.1:p.Glu802Ala
XM_011512866.1:c.2354A>C	XP_011511168.1:p.Glu785Ala
XM_011512867.1:c.2351A>C	XP_011511169.1:p.Glu784Ala
XM_011512868.1:c.2243A>C	XP_011511170.1:p.Glu748Ala
XR_924835.1:n.582+9363T>G
NM_001354663.1:c.1982A>C	NP_001341592.1:p.Glu661Ala
NM_001354664.1:c.1979A>C	NP_001341593.1:p.Glu660Ala
XR_001740158.2:n.2770A>C
XR_001740159.2:n.2605A>C
XR_001741074.1:n.475+11251T>G
XR_924835.2:n.600+9363T>G
NM_001354663.2:c.1982A>C	NP_001341592.1:p.Glu661Ala
NM_001354664.2:c.1979A>C	NP_001341593.1:p.Glu660Ala
NM_130831.3:c.2243A>C	NP_570844.1:p.Glu748Ala
NM_130832.3:c.2297A>C	NP_570845.1:p.Glu766Ala
NM_130834.3:c.2405A>C	NP_570847.2:p.Glu802Ala
NM_130836.3:c.2462A>C	NP_570849.2:p.Glu821Ala
NM_015560.3:c.2351A>C	NP_056375.2:p.Glu784Ala
NM_130833.3:c.2354A>C	NP_570846.1:p.Glu785Ala
NM_130835.3:c.2408A>C	NP_570848.1:p.Glu803Ala
NM_130837.3:c.2516A>C MANE Select	NP_570850.2:p.Glu839Ala