Canonical Allele Identifier: CA355797259

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193384986A>G (hg19) ; chr3:g.193667197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193667197A>G , CM000665.2:g.193667197A>G	GRCh38
NC_000003.11:g.193384986A>G , CM000665.1:g.193384986A>G	GRCh37
NC_000003.10:g.194867680A>G	NCBI36
NG_011605.1:g.79054A>G , LRG_337:g.79054A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2900A>G MANE Select	ENSP00000355324.2:p.Glu967Gly
ENST00000361828.7:c.2735A>G	ENSP00000354429.3:p.Glu912Gly
ENST00000361908.8:c.2846A>G	ENSP00000354681.3:p.Glu949Gly
ENST00000392436.7:c.2735A>G	ENSP00000376231.3:p.Glu912Gly
ENST00000392437.6:c.2789A>G	ENSP00000376232.2:p.Glu930Gly
ENST00000642289.1:c.2674A>G
ENST00000642445.1:c.2735A>G	ENSP00000495535.1:p.Glu912Gly
ENST00000642593.1:c.*960A>G	ENSP00000494273.1:n.*960A>G
ENST00000643329.1:c.2417A>G	ENSP00000493673.1:p.Glu806Gly
ENST00000643737.1:c.*2816A>G	ENSP00000494210.1:n.*2816A>G
ENST00000644595.1:c.2735A>G	ENSP00000494121.1:p.Glu912Gly
ENST00000644629.1:c.2322A>G
ENST00000644841.1:c.*1219A>G	ENSP00000493988.1:n.*1219A>G
ENST00000644959.1:c.2729A>G
ENST00000645553.1:c.2750A>G	ENSP00000494725.1:p.Glu917Gly
ENST00000646085.1:c.*2213A>G	ENSP00000494509.1:n.*2213A>G
ENST00000646277.1:c.*1336A>G	ENSP00000495289.1:n.*1336A>G
ENST00000646544.1:c.1723A>G
ENST00000646699.1:c.2674A>G
ENST00000646793.1:c.2627A>G	ENSP00000494512.1:p.Glu876Gly
ENST00000361150.6:c.2738A>G	ENSP00000354781.2:p.Glu913Gly
ENST00000361510.6:c.2900A>G	ENSP00000355324.2:p.Glu967Gly
ENST00000361715.6:c.2792A>G	ENSP00000355311.2:p.Glu931Gly
ENST00000361828.6:c.2789A>G	ENSP00000354429.2:p.Glu930Gly
ENST00000361908.7:c.2846A>G	ENSP00000354681.3:p.Glu949Gly
ENST00000392438.7:c.2735A>G	ENSP00000376233.3:p.Glu912Gly
ENST00000429164.1:c.22A>G
ENST00000445863.1:c.311A>G	ENSP00000398358.1:p.Glu104Gly
NM_015560.2:c.2735A>G , LRG_337t1:c.2735A>G	NP_056375.2:p.Glu912Gly
NM_130831.2:c.2627A>G	NP_570844.1:p.Glu876Gly
NM_130832.2:c.2681A>G	NP_570845.1:p.Glu894Gly
NM_130833.2:c.2738A>G	NP_570846.1:p.Glu913Gly
NM_130834.2:c.2789A>G	NP_570847.2:p.Glu930Gly
NM_130835.2:c.2792A>G	NP_570848.1:p.Glu931Gly
NM_130836.2:c.2846A>G	NP_570849.2:p.Glu949Gly
NM_130837.2:c.2900A>G , LRG_337t2:c.2900A>G	NP_570850.2:p.Glu967Gly
XM_011512863.1:c.2900A>G	XP_011511165.1:p.Glu967Gly
XM_011512864.1:c.2846A>G	XP_011511166.1:p.Glu949Gly
XM_011512865.1:c.2789A>G	XP_011511167.1:p.Glu930Gly
XM_011512866.1:c.2738A>G	XP_011511168.1:p.Glu913Gly
XM_011512867.1:c.2735A>G	XP_011511169.1:p.Glu912Gly
XM_011512868.1:c.2627A>G	XP_011511170.1:p.Glu876Gly
XR_924835.1:n.582+1723T>C
NM_001354663.1:c.2366A>G	NP_001341592.1:p.Glu789Gly
NM_001354664.1:c.2363A>G	NP_001341593.1:p.Glu788Gly
XR_001740158.2:n.3154A>G
XR_001740159.2:n.2989A>G
XR_001741072.1:n.600+1723T>C
XR_001741074.1:n.475+3611T>C
XR_924835.2:n.600+1723T>C
NM_001354663.2:c.2366A>G	NP_001341592.1:p.Glu789Gly
NM_001354664.2:c.2363A>G	NP_001341593.1:p.Glu788Gly
NM_130831.3:c.2627A>G	NP_570844.1:p.Glu876Gly
NM_130832.3:c.2681A>G	NP_570845.1:p.Glu894Gly
NM_130834.3:c.2789A>G	NP_570847.2:p.Glu930Gly
NM_130836.3:c.2846A>G	NP_570849.2:p.Glu949Gly
NM_015560.3:c.2735A>G	NP_056375.2:p.Glu912Gly
NM_130833.3:c.2738A>G	NP_570846.1:p.Glu913Gly
NM_130835.3:c.2792A>G	NP_570848.1:p.Glu931Gly
NM_130837.3:c.2900A>G MANE Select	NP_570850.2:p.Glu967Gly