Canonical Allele Identifier: CA437441543

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377341C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659552C>G , CM000665.2:g.193659552C>G	GRCh38
NC_000003.11:g.193377341C>G , CM000665.1:g.193377341C>G	GRCh37
NC_000003.10:g.194860035C>G	NCBI36
NG_011605.1:g.71409C>G , LRG_337:g.71409C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2511C>G MANE Select	ENSP00000355324.2:p.Thr837=
ENST00000361828.7:c.2346C>G	ENSP00000354429.3:p.Thr782=
ENST00000361908.8:c.2457C>G	ENSP00000354681.3:p.Thr819=
ENST00000392436.7:c.2346C>G	ENSP00000376231.3:p.Thr782=
ENST00000392437.6:c.2400C>G	ENSP00000376232.2:p.Thr800=
ENST00000642289.1:c.2285C>G
ENST00000642445.1:c.2346C>G	ENSP00000495535.1:p.Thr782=
ENST00000642593.1:c.*571C>G	ENSP00000494273.1:n.*571C>G
ENST00000643329.1:c.2028C>G	ENSP00000493673.1:p.Thr676=
ENST00000643737.1:c.*2427C>G	ENSP00000494210.1:n.*2427C>G
ENST00000644595.1:c.2346C>G	ENSP00000494121.1:p.Thr782=
ENST00000644629.1:c.1933C>G
ENST00000644841.1:c.*830C>G	ENSP00000493988.1:n.*830C>G
ENST00000644959.1:c.2340C>G
ENST00000645553.1:c.2361C>G	ENSP00000494725.1:p.Thr787=
ENST00000646085.1:c.*1824C>G	ENSP00000494509.1:n.*1824C>G
ENST00000646277.1:c.*947C>G	ENSP00000495289.1:n.*947C>G
ENST00000646544.1:c.1334C>G
ENST00000646699.1:c.2285C>G
ENST00000646793.1:c.2238C>G	ENSP00000494512.1:p.Thr746=
ENST00000361150.6:c.2349C>G	ENSP00000354781.2:p.Thr783=
ENST00000361510.6:c.2511C>G	ENSP00000355324.2:p.Thr837=
ENST00000361715.6:c.2403C>G	ENSP00000355311.2:p.Thr801=
ENST00000361828.6:c.2400C>G	ENSP00000354429.2:p.Thr800=
ENST00000361908.7:c.2457C>G	ENSP00000354681.3:p.Thr819=
ENST00000392438.7:c.2346C>G	ENSP00000376233.3:p.Thr782=
NM_015560.2:c.2346C>G , LRG_337t1:c.2346C>G	NP_056375.2:p.Thr782=
NM_130831.2:c.2238C>G	NP_570844.1:p.Thr746=
NM_130832.2:c.2292C>G	NP_570845.1:p.Thr764=
NM_130833.2:c.2349C>G	NP_570846.1:p.Thr783=
NM_130834.2:c.2400C>G	NP_570847.2:p.Thr800=
NM_130835.2:c.2403C>G	NP_570848.1:p.Thr801=
NM_130836.2:c.2457C>G	NP_570849.2:p.Thr819=
NM_130837.2:c.2511C>G , LRG_337t2:c.2511C>G	NP_570850.2:p.Thr837=
XM_011512863.1:c.2511C>G	XP_011511165.1:p.Thr837=
XM_011512864.1:c.2457C>G	XP_011511166.1:p.Thr819=
XM_011512865.1:c.2400C>G	XP_011511167.1:p.Thr800=
XM_011512866.1:c.2349C>G	XP_011511168.1:p.Thr783=
XM_011512867.1:c.2346C>G	XP_011511169.1:p.Thr782=
XM_011512868.1:c.2238C>G	XP_011511170.1:p.Thr746=
XR_924835.1:n.582+9368G>C
NM_001354663.1:c.1977C>G	NP_001341592.1:p.Thr659=
NM_001354664.1:c.1974C>G	NP_001341593.1:p.Thr658=
XR_001740158.2:n.2765C>G
XR_001740159.2:n.2600C>G
XR_001741074.1:n.475+11256G>C
XR_924835.2:n.600+9368G>C
NM_001354663.2:c.1977C>G	NP_001341592.1:p.Thr659=
NM_001354664.2:c.1974C>G	NP_001341593.1:p.Thr658=
NM_130831.3:c.2238C>G	NP_570844.1:p.Thr746=
NM_130832.3:c.2292C>G	NP_570845.1:p.Thr764=
NM_130834.3:c.2400C>G	NP_570847.2:p.Thr800=
NM_130836.3:c.2457C>G	NP_570849.2:p.Thr819=
NM_015560.3:c.2346C>G	NP_056375.2:p.Thr782=
NM_130833.3:c.2349C>G	NP_570846.1:p.Thr783=
NM_130835.3:c.2403C>G	NP_570848.1:p.Thr801=
NM_130837.3:c.2511C>G MANE Select	NP_570850.2:p.Thr837=