Canonical Allele Identifier: CA2759264

Gene: OPA1

Linked Data

• ClinVar Variation Id: 2905648
• ClinVar RCV Id: RCV003731808
• dbSNP Id: rs775371840
• ExAC: 3:193355833 G / A
• gnomAD v2: 3-193355833-G-A
• gnomAD v4: 3-193638044-G-A
• MyVariant Identifiers: chr3:g.193355833G>A (hg19) ; chr3:g.193638044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193638044G>A , CM000665.2:g.193638044G>A	GRCh38
NC_000003.11:g.193355833G>A , CM000665.1:g.193355833G>A	GRCh37
NC_000003.10:g.194838527G>A	NCBI36
NG_011605.1:g.49901G>A , LRG_337:g.49901G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1128G>A MANE Select	ENSP00000355324.2:p.Met376Ile
ENST00000361828.7:c.963G>A	ENSP00000354429.3:p.Met321Ile
ENST00000361908.8:c.1074G>A	ENSP00000354681.3:p.Met358Ile
ENST00000392436.7:c.963G>A	ENSP00000376231.3:p.Met321Ile
ENST00000392437.6:c.1017G>A	ENSP00000376232.2:p.Met339Ile
ENST00000642289.1:c.1058G>A
ENST00000642445.1:c.963G>A	ENSP00000495535.1:p.Met321Ile
ENST00000642593.1:c.963G>A	ENSP00000494273.1:p.Met321Ile
ENST00000643329.1:c.645G>A	ENSP00000493673.1:p.Met215Ile
ENST00000643737.1:c.*1044G>A	ENSP00000494210.1:n.*1044G>A
ENST00000644595.1:c.963G>A	ENSP00000494121.1:p.Met321Ile
ENST00000644629.1:c.623G>A
ENST00000644841.1:c.591G>A	ENSP00000493988.1:p.Met197Ile
ENST00000644959.1:c.932G>A
ENST00000645553.1:c.978G>A	ENSP00000494725.1:p.Met326Ile
ENST00000646085.1:c.*441G>A	ENSP00000494509.1:n.*441G>A
ENST00000646277.1:c.1128G>A	ENSP00000495289.1:p.Met376Ile
ENST00000646544.1:c.26G>A
ENST00000646699.1:c.1058G>A
ENST00000646793.1:c.855G>A	ENSP00000494512.1:p.Met285Ile
ENST00000361150.6:c.966G>A	ENSP00000354781.2:p.Met322Ile
ENST00000361510.6:c.1128G>A	ENSP00000355324.2:p.Met376Ile
ENST00000361715.6:c.1020G>A	ENSP00000355311.2:p.Met340Ile
ENST00000361828.6:c.1017G>A	ENSP00000354429.2:p.Met339Ile
ENST00000361908.7:c.1074G>A	ENSP00000354681.3:p.Met358Ile
ENST00000392438.7:c.963G>A	ENSP00000376233.3:p.Met321Ile
ENST00000475899.1:n.159G>A
ENST00000495476.1:n.484G>A
ENST00000497189.5:n.449G>A
NM_015560.2:c.963G>A , LRG_337t1:c.963G>A	NP_056375.2:p.Met321Ile
NM_130831.2:c.855G>A	NP_570844.1:p.Met285Ile
NM_130832.2:c.909G>A	NP_570845.1:p.Met303Ile
NM_130833.2:c.966G>A	NP_570846.1:p.Met322Ile
NM_130834.2:c.1017G>A	NP_570847.2:p.Met339Ile
NM_130835.2:c.1020G>A	NP_570848.1:p.Met340Ile
NM_130836.2:c.1074G>A	NP_570849.2:p.Met358Ile
NM_130837.2:c.1128G>A , LRG_337t2:c.1128G>A	NP_570850.2:p.Met376Ile
XM_011512863.1:c.1128G>A	XP_011511165.1:p.Met376Ile
XM_011512864.1:c.1074G>A	XP_011511166.1:p.Met358Ile
XM_011512865.1:c.1017G>A	XP_011511167.1:p.Met339Ile
XM_011512866.1:c.966G>A	XP_011511168.1:p.Met322Ile
XM_011512867.1:c.963G>A	XP_011511169.1:p.Met321Ile
XM_011512868.1:c.855G>A	XP_011511170.1:p.Met285Ile
XM_011512869.1:c.1128G>A	XP_011511171.1:p.Met376Ile
NM_001354663.1:c.594G>A	NP_001341592.1:p.Met198Ile
NM_001354664.1:c.591G>A	NP_001341593.1:p.Met197Ile
XR_001740158.2:n.1357G>A
XR_001740159.2:n.1192G>A
NM_001354663.2:c.594G>A	NP_001341592.1:p.Met198Ile
NM_001354664.2:c.591G>A	NP_001341593.1:p.Met197Ile
NM_130831.3:c.855G>A	NP_570844.1:p.Met285Ile
NM_130832.3:c.909G>A	NP_570845.1:p.Met303Ile
NM_130834.3:c.1017G>A	NP_570847.2:p.Met339Ile
NM_130836.3:c.1074G>A	NP_570849.2:p.Met358Ile
NM_015560.3:c.963G>A	NP_056375.2:p.Met321Ile
NM_130833.3:c.966G>A	NP_570846.1:p.Met322Ile
NM_130835.3:c.1020G>A	NP_570848.1:p.Met340Ile
NM_130837.3:c.1128G>A MANE Select	NP_570850.2:p.Met376Ile