Canonical Allele Identifier: CA355790599

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193364966A>G (hg19) ; chr3:g.193647177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647177A>G , CM000665.2:g.193647177A>G	GRCh38
NC_000003.11:g.193364966A>G , CM000665.1:g.193364966A>G	GRCh37
NC_000003.10:g.194847660A>G	NCBI36
NG_011605.1:g.59034A>G , LRG_337:g.59034A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1867A>G MANE Select	ENSP00000355324.2:p.Lys623Glu
ENST00000361828.7:c.1702A>G	ENSP00000354429.3:p.Lys568Glu
ENST00000361908.8:c.1813A>G	ENSP00000354681.3:p.Lys605Glu
ENST00000392436.7:c.1702A>G	ENSP00000376231.3:p.Lys568Glu
ENST00000392437.6:c.1756A>G	ENSP00000376232.2:p.Lys586Glu
ENST00000642289.1:c.1641A>G
ENST00000642445.1:c.1702A>G	ENSP00000495535.1:p.Lys568Glu
ENST00000642593.1:c.1702A>G	ENSP00000494273.1:p.Lys568Glu
ENST00000643329.1:c.1384A>G	ENSP00000493673.1:p.Lys462Glu
ENST00000643737.1:c.*1783A>G	ENSP00000494210.1:n.*1783A>G
ENST00000644595.1:c.1702A>G	ENSP00000494121.1:p.Lys568Glu
ENST00000644629.1:c.1289A>G
ENST00000644841.1:c.*186A>G	ENSP00000493988.1:n.*186A>G
ENST00000644959.1:c.1671A>G
ENST00000645553.1:c.1717A>G	ENSP00000494725.1:p.Lys573Glu
ENST00000646085.1:c.*1180A>G	ENSP00000494509.1:n.*1180A>G
ENST00000646277.1:c.*303A>G	ENSP00000495289.1:n.*303A>G
ENST00000646544.1:c.690A>G
ENST00000646699.1:c.1641A>G
ENST00000646793.1:c.1594A>G	ENSP00000494512.1:p.Lys532Glu
ENST00000361150.6:c.1705A>G	ENSP00000354781.2:p.Lys569Glu
ENST00000361510.6:c.1867A>G	ENSP00000355324.2:p.Lys623Glu
ENST00000361715.6:c.1759A>G	ENSP00000355311.2:p.Lys587Glu
ENST00000361828.6:c.1756A>G	ENSP00000354429.2:p.Lys586Glu
ENST00000361908.7:c.1813A>G	ENSP00000354681.3:p.Lys605Glu
ENST00000392438.7:c.1702A>G	ENSP00000376233.3:p.Lys568Glu
ENST00000483516.1:n.200A>G
NM_015560.2:c.1702A>G , LRG_337t1:c.1702A>G	NP_056375.2:p.Lys568Glu
NM_130831.2:c.1594A>G	NP_570844.1:p.Lys532Glu
NM_130832.2:c.1648A>G	NP_570845.1:p.Lys550Glu
NM_130833.2:c.1705A>G	NP_570846.1:p.Lys569Glu
NM_130834.2:c.1756A>G	NP_570847.2:p.Lys586Glu
NM_130835.2:c.1759A>G	NP_570848.1:p.Lys587Glu
NM_130836.2:c.1813A>G	NP_570849.2:p.Lys605Glu
NM_130837.2:c.1867A>G , LRG_337t2:c.1867A>G	NP_570850.2:p.Lys623Glu
XM_011512863.1:c.1867A>G	XP_011511165.1:p.Lys623Glu
XM_011512864.1:c.1813A>G	XP_011511166.1:p.Lys605Glu
XM_011512865.1:c.1756A>G	XP_011511167.1:p.Lys586Glu
XM_011512866.1:c.1705A>G	XP_011511168.1:p.Lys569Glu
XM_011512867.1:c.1702A>G	XP_011511169.1:p.Lys568Glu
XM_011512868.1:c.1594A>G	XP_011511170.1:p.Lys532Glu
XM_011512869.1:c.1867A>G	XP_011511171.1:p.Lys623Glu
NM_001354663.1:c.1333A>G	NP_001341592.1:p.Lys445Glu
NM_001354664.1:c.1330A>G	NP_001341593.1:p.Lys444Glu
XR_001740158.2:n.2096A>G
XR_001740159.2:n.1931A>G
NM_001354663.2:c.1333A>G	NP_001341592.1:p.Lys445Glu
NM_001354664.2:c.1330A>G	NP_001341593.1:p.Lys444Glu
NM_130831.3:c.1594A>G	NP_570844.1:p.Lys532Glu
NM_130832.3:c.1648A>G	NP_570845.1:p.Lys550Glu
NM_130834.3:c.1756A>G	NP_570847.2:p.Lys586Glu
NM_130836.3:c.1813A>G	NP_570849.2:p.Lys605Glu
NM_015560.3:c.1702A>G	NP_056375.2:p.Lys568Glu
NM_130833.3:c.1705A>G	NP_570846.1:p.Lys569Glu
NM_130835.3:c.1759A>G	NP_570848.1:p.Lys587Glu
NM_130837.3:c.1867A>G MANE Select	NP_570850.2:p.Lys623Glu