Canonical Allele Identifier: CA2759263

Gene: OPA1

Linked Data

• ClinVar Variation Id: 2713156
• ClinVar RCV Id: RCV003548283
• dbSNP Id: rs771817617
• ExAC: 3:193355809 A / G
• gnomAD v2: 3-193355809-A-G
• gnomAD v3: 3-193638020-A-G
• gnomAD v4: 3-193638020-A-G
• MyVariant Identifiers: chr3:g.193355809A>G (hg19) ; chr3:g.193638020A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193638020A>G , CM000665.2:g.193638020A>G	GRCh38
NC_000003.11:g.193355809A>G , CM000665.1:g.193355809A>G	GRCh37
NC_000003.10:g.194838503A>G	NCBI36
NG_011605.1:g.49877A>G , LRG_337:g.49877A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1104A>G MANE Select	ENSP00000355324.2:p.Ile368Met
ENST00000361828.7:c.939A>G	ENSP00000354429.3:p.Ile313Met
ENST00000361908.8:c.1050A>G	ENSP00000354681.3:p.Ile350Met
ENST00000392436.7:c.939A>G	ENSP00000376231.3:p.Ile313Met
ENST00000392437.6:c.993A>G	ENSP00000376232.2:p.Ile331Met
ENST00000642289.1:c.1034A>G
ENST00000642445.1:c.939A>G	ENSP00000495535.1:p.Ile313Met
ENST00000642593.1:c.939A>G	ENSP00000494273.1:p.Ile313Met
ENST00000643329.1:c.621A>G	ENSP00000493673.1:p.Ile207Met
ENST00000643737.1:c.*1020A>G	ENSP00000494210.1:n.*1020A>G
ENST00000644595.1:c.939A>G	ENSP00000494121.1:p.Ile313Met
ENST00000644629.1:c.599A>G
ENST00000644841.1:c.567A>G	ENSP00000493988.1:p.Ile189Met
ENST00000644959.1:c.908A>G
ENST00000645553.1:c.954A>G	ENSP00000494725.1:p.Ile318Met
ENST00000646085.1:c.*417A>G	ENSP00000494509.1:n.*417A>G
ENST00000646277.1:c.1104A>G	ENSP00000495289.1:p.Ile368Met
ENST00000646544.1:c.2A>G
ENST00000646699.1:c.1034A>G
ENST00000646793.1:c.831A>G	ENSP00000494512.1:p.Ile277Met
ENST00000361150.6:c.942A>G	ENSP00000354781.2:p.Ile314Met
ENST00000361510.6:c.1104A>G	ENSP00000355324.2:p.Ile368Met
ENST00000361715.6:c.996A>G	ENSP00000355311.2:p.Ile332Met
ENST00000361828.6:c.993A>G	ENSP00000354429.2:p.Ile331Met
ENST00000361908.7:c.1050A>G	ENSP00000354681.3:p.Ile350Met
ENST00000392438.7:c.939A>G	ENSP00000376233.3:p.Ile313Met
ENST00000475899.1:n.135A>G
ENST00000495476.1:n.460A>G
ENST00000497189.5:n.425A>G
NM_015560.2:c.939A>G , LRG_337t1:c.939A>G	NP_056375.2:p.Ile313Met
NM_130831.2:c.831A>G	NP_570844.1:p.Ile277Met
NM_130832.2:c.885A>G	NP_570845.1:p.Ile295Met
NM_130833.2:c.942A>G	NP_570846.1:p.Ile314Met
NM_130834.2:c.993A>G	NP_570847.2:p.Ile331Met
NM_130835.2:c.996A>G	NP_570848.1:p.Ile332Met
NM_130836.2:c.1050A>G	NP_570849.2:p.Ile350Met
NM_130837.2:c.1104A>G , LRG_337t2:c.1104A>G	NP_570850.2:p.Ile368Met
XM_011512863.1:c.1104A>G	XP_011511165.1:p.Ile368Met
XM_011512864.1:c.1050A>G	XP_011511166.1:p.Ile350Met
XM_011512865.1:c.993A>G	XP_011511167.1:p.Ile331Met
XM_011512866.1:c.942A>G	XP_011511168.1:p.Ile314Met
XM_011512867.1:c.939A>G	XP_011511169.1:p.Ile313Met
XM_011512868.1:c.831A>G	XP_011511170.1:p.Ile277Met
XM_011512869.1:c.1104A>G	XP_011511171.1:p.Ile368Met
NM_001354663.1:c.570A>G	NP_001341592.1:p.Ile190Met
NM_001354664.1:c.567A>G	NP_001341593.1:p.Ile189Met
XR_001740158.2:n.1333A>G
XR_001740159.2:n.1168A>G
NM_001354663.2:c.570A>G	NP_001341592.1:p.Ile190Met
NM_001354664.2:c.567A>G	NP_001341593.1:p.Ile189Met
NM_130831.3:c.831A>G	NP_570844.1:p.Ile277Met
NM_130832.3:c.885A>G	NP_570845.1:p.Ile295Met
NM_130834.3:c.993A>G	NP_570847.2:p.Ile331Met
NM_130836.3:c.1050A>G	NP_570849.2:p.Ile350Met
NM_015560.3:c.939A>G	NP_056375.2:p.Ile313Met
NM_130833.3:c.942A>G	NP_570846.1:p.Ile314Met
NM_130835.3:c.996A>G	NP_570848.1:p.Ile332Met
NM_130837.3:c.1104A>G MANE Select	NP_570850.2:p.Ile368Met