Canonical Allele Identifier: CA347676

Gene: OPA1

Linked Data

• ClinVar Variation Id: 217842
• ClinVar RCV Id: RCV000201900
• dbSNP Id: rs863225276
• MyVariant Identifiers: chr3:g.193361223G>A (hg19) ; chr3:g.193643434G>A (hg38)
• PubMed: PMID:20301426 ; PMID:23384603

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643434G>A , CM000665.2:g.193643434G>A	GRCh38
NC_000003.11:g.193361223G>A , CM000665.1:g.193361223G>A	GRCh37
NC_000003.10:g.194843917G>A	NCBI36
NG_011605.1:g.55291G>A , LRG_337:g.55291G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1367G>A MANE Select	ENSP00000355324.2:p.Gly456Asp
ENST00000361828.7:c.1202G>A	ENSP00000354429.3:p.Gly401Asp
ENST00000361908.8:c.1313G>A	ENSP00000354681.3:p.Gly438Asp
ENST00000392436.7:c.1202G>A	ENSP00000376231.3:p.Gly401Asp
ENST00000392437.6:c.1256G>A	ENSP00000376232.2:p.Gly419Asp
ENST00000642289.1:c.1141G>A
ENST00000642445.1:c.1202G>A	ENSP00000495535.1:p.Gly401Asp
ENST00000642593.1:c.1202G>A	ENSP00000494273.1:p.Gly401Asp
ENST00000643329.1:c.884G>A	ENSP00000493673.1:p.Gly295Asp
ENST00000643737.1:c.*1283G>A	ENSP00000494210.1:n.*1283G>A
ENST00000644595.1:c.1202G>A	ENSP00000494121.1:p.Gly401Asp
ENST00000644629.1:c.862G>A
ENST00000644841.1:c.830G>A	ENSP00000493988.1:p.Gly277Asp
ENST00000644959.1:c.1171G>A
ENST00000645553.1:c.1217G>A	ENSP00000494725.1:p.Gly406Asp
ENST00000646085.1:c.*680G>A	ENSP00000494509.1:n.*680G>A
ENST00000646277.1:c.1367G>A	ENSP00000495289.1:p.Gly456Asp
ENST00000646544.1:c.190G>A
ENST00000646699.1:c.1141G>A
ENST00000646793.1:c.1094G>A	ENSP00000494512.1:p.Gly365Asp
ENST00000361150.6:c.1205G>A	ENSP00000354781.2:p.Gly402Asp
ENST00000361510.6:c.1367G>A	ENSP00000355324.2:p.Gly456Asp
ENST00000361715.6:c.1259G>A	ENSP00000355311.2:p.Gly420Asp
ENST00000361828.6:c.1256G>A	ENSP00000354429.2:p.Gly419Asp
ENST00000361908.7:c.1313G>A	ENSP00000354681.3:p.Gly438Asp
ENST00000392438.7:c.1202G>A	ENSP00000376233.3:p.Gly401Asp
ENST00000475899.1:n.398G>A
NM_015560.2:c.1202G>A , LRG_337t1:c.1202G>A	NP_056375.2:p.Gly401Asp
NM_130831.2:c.1094G>A	NP_570844.1:p.Gly365Asp
NM_130832.2:c.1148G>A	NP_570845.1:p.Gly383Asp
NM_130833.2:c.1205G>A	NP_570846.1:p.Gly402Asp
NM_130834.2:c.1256G>A	NP_570847.2:p.Gly419Asp
NM_130835.2:c.1259G>A	NP_570848.1:p.Gly420Asp
NM_130836.2:c.1313G>A	NP_570849.2:p.Gly438Asp
NM_130837.2:c.1367G>A , LRG_337t2:c.1367G>A	NP_570850.2:p.Gly456Asp
XM_011512863.1:c.1367G>A	XP_011511165.1:p.Gly456Asp
XM_011512864.1:c.1313G>A	XP_011511166.1:p.Gly438Asp
XM_011512865.1:c.1256G>A	XP_011511167.1:p.Gly419Asp
XM_011512866.1:c.1205G>A	XP_011511168.1:p.Gly402Asp
XM_011512867.1:c.1202G>A	XP_011511169.1:p.Gly401Asp
XM_011512868.1:c.1094G>A	XP_011511170.1:p.Gly365Asp
XM_011512869.1:c.1367G>A	XP_011511171.1:p.Gly456Asp
NM_001354663.1:c.833G>A	NP_001341592.1:p.Gly278Asp
NM_001354664.1:c.830G>A	NP_001341593.1:p.Gly277Asp
XR_001740158.2:n.1596G>A
XR_001740159.2:n.1431G>A
NM_001354663.2:c.833G>A	NP_001341592.1:p.Gly278Asp
NM_001354664.2:c.830G>A	NP_001341593.1:p.Gly277Asp
NM_130831.3:c.1094G>A	NP_570844.1:p.Gly365Asp
NM_130832.3:c.1148G>A	NP_570845.1:p.Gly383Asp
NM_130834.3:c.1256G>A	NP_570847.2:p.Gly419Asp
NM_130836.3:c.1313G>A	NP_570849.2:p.Gly438Asp
NM_015560.3:c.1202G>A	NP_056375.2:p.Gly401Asp
NM_130833.3:c.1205G>A	NP_570846.1:p.Gly402Asp
NM_130835.3:c.1259G>A	NP_570848.1:p.Gly420Asp
NM_130837.3:c.1367G>A MANE Select	NP_570850.2:p.Gly456Asp