Canonical Allele Identifier: CA355788122

Gene: OPA1

Linked Data

• ClinVar Variation Id: 1398078
• ClinVar RCV Id: RCV001912748
• dbSNP Id: rs2109014867
• MyVariant Identifiers: chr3:g.193355744G>T (hg19) ; chr3:g.193637955G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193637955G>T , CM000665.2:g.193637955G>T	GRCh38
NC_000003.11:g.193355744G>T , CM000665.1:g.193355744G>T	GRCh37
NC_000003.10:g.194838438G>T	NCBI36
NG_011605.1:g.49812G>T , LRG_337:g.49812G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1039G>T MANE Select	ENSP00000355324.2:p.Val347Phe
ENST00000361828.7:c.874G>T	ENSP00000354429.3:p.Val292Phe
ENST00000361908.8:c.985G>T	ENSP00000354681.3:p.Val329Phe
ENST00000392436.7:c.874G>T	ENSP00000376231.3:p.Val292Phe
ENST00000392437.6:c.928G>T	ENSP00000376232.2:p.Val310Phe
ENST00000642289.1:c.969G>T
ENST00000642445.1:c.874G>T	ENSP00000495535.1:p.Val292Phe
ENST00000642593.1:c.874G>T	ENSP00000494273.1:p.Val292Phe
ENST00000643329.1:c.556G>T	ENSP00000493673.1:p.Val186Phe
ENST00000643737.1:c.*955G>T	ENSP00000494210.1:n.*955G>T
ENST00000644595.1:c.874G>T	ENSP00000494121.1:p.Val292Phe
ENST00000644629.1:c.534G>T
ENST00000644841.1:c.502G>T	ENSP00000493988.1:p.Val168Phe
ENST00000644959.1:c.843G>T
ENST00000645553.1:c.889G>T	ENSP00000494725.1:p.Val297Phe
ENST00000646085.1:c.*352G>T	ENSP00000494509.1:n.*352G>T
ENST00000646277.1:c.1039G>T	ENSP00000495289.1:p.Val347Phe
ENST00000646699.1:c.969G>T
ENST00000646793.1:c.766G>T	ENSP00000494512.1:p.Val256Phe
ENST00000361150.6:c.877G>T	ENSP00000354781.2:p.Val293Phe
ENST00000361510.6:c.1039G>T	ENSP00000355324.2:p.Val347Phe
ENST00000361715.6:c.931G>T	ENSP00000355311.2:p.Val311Phe
ENST00000361828.6:c.928G>T	ENSP00000354429.2:p.Val310Phe
ENST00000361908.7:c.985G>T	ENSP00000354681.3:p.Val329Phe
ENST00000392438.7:c.874G>T	ENSP00000376233.3:p.Val292Phe
ENST00000475899.1:n.70G>T
ENST00000495476.1:n.395G>T
ENST00000497189.5:n.360G>T
NM_015560.2:c.874G>T , LRG_337t1:c.874G>T	NP_056375.2:p.Val292Phe
NM_130831.2:c.766G>T	NP_570844.1:p.Val256Phe
NM_130832.2:c.820G>T	NP_570845.1:p.Val274Phe
NM_130833.2:c.877G>T	NP_570846.1:p.Val293Phe
NM_130834.2:c.928G>T	NP_570847.2:p.Val310Phe
NM_130835.2:c.931G>T	NP_570848.1:p.Val311Phe
NM_130836.2:c.985G>T	NP_570849.2:p.Val329Phe
NM_130837.2:c.1039G>T , LRG_337t2:c.1039G>T	NP_570850.2:p.Val347Phe
XM_011512863.1:c.1039G>T	XP_011511165.1:p.Val347Phe
XM_011512864.1:c.985G>T	XP_011511166.1:p.Val329Phe
XM_011512865.1:c.928G>T	XP_011511167.1:p.Val310Phe
XM_011512866.1:c.877G>T	XP_011511168.1:p.Val293Phe
XM_011512867.1:c.874G>T	XP_011511169.1:p.Val292Phe
XM_011512868.1:c.766G>T	XP_011511170.1:p.Val256Phe
XM_011512869.1:c.1039G>T	XP_011511171.1:p.Val347Phe
NM_001354663.1:c.505G>T	NP_001341592.1:p.Val169Phe
NM_001354664.1:c.502G>T	NP_001341593.1:p.Val168Phe
XR_001740158.2:n.1268G>T
XR_001740159.2:n.1103G>T
NM_001354663.2:c.505G>T	NP_001341592.1:p.Val169Phe
NM_001354664.2:c.502G>T	NP_001341593.1:p.Val168Phe
NM_130831.3:c.766G>T	NP_570844.1:p.Val256Phe
NM_130832.3:c.820G>T	NP_570845.1:p.Val274Phe
NM_130834.3:c.928G>T	NP_570847.2:p.Val310Phe
NM_130836.3:c.985G>T	NP_570849.2:p.Val329Phe
NM_015560.3:c.874G>T	NP_056375.2:p.Val292Phe
NM_130833.3:c.877G>T	NP_570846.1:p.Val293Phe
NM_130835.3:c.931G>T	NP_570848.1:p.Val311Phe
NM_130837.3:c.1039G>T MANE Select	NP_570850.2:p.Val347Phe