Canonical Allele Identifier: CA437437501

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193364866A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647077A>T , CM000665.2:g.193647077A>T	GRCh38
NC_000003.11:g.193364866A>T , CM000665.1:g.193364866A>T	GRCh37
NC_000003.10:g.194847560A>T	NCBI36
NG_011605.1:g.58934A>T , LRG_337:g.58934A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1767A>T MANE Select	ENSP00000355324.2:p.Leu589=
ENST00000361828.7:c.1602A>T	ENSP00000354429.3:p.Leu534=
ENST00000361908.8:c.1713A>T	ENSP00000354681.3:p.Leu571=
ENST00000392436.7:c.1602A>T	ENSP00000376231.3:p.Leu534=
ENST00000392437.6:c.1656A>T	ENSP00000376232.2:p.Leu552=
ENST00000642289.1:c.1541A>T
ENST00000642445.1:c.1602A>T	ENSP00000495535.1:p.Leu534=
ENST00000642593.1:c.1602A>T	ENSP00000494273.1:p.Leu534=
ENST00000643329.1:c.1284A>T	ENSP00000493673.1:p.Leu428=
ENST00000643737.1:c.*1683A>T	ENSP00000494210.1:n.*1683A>T
ENST00000644595.1:c.1602A>T	ENSP00000494121.1:p.Leu534=
ENST00000644629.1:c.1189A>T
ENST00000644841.1:c.*86A>T	ENSP00000493988.1:n.*86A>T
ENST00000644959.1:c.1571A>T
ENST00000645553.1:c.1617A>T	ENSP00000494725.1:p.Leu539=
ENST00000646085.1:c.*1080A>T	ENSP00000494509.1:n.*1080A>T
ENST00000646277.1:c.*203A>T	ENSP00000495289.1:n.*203A>T
ENST00000646544.1:c.590A>T
ENST00000646699.1:c.1541A>T
ENST00000646793.1:c.1494A>T	ENSP00000494512.1:p.Leu498=
ENST00000361150.6:c.1605A>T	ENSP00000354781.2:p.Leu535=
ENST00000361510.6:c.1767A>T	ENSP00000355324.2:p.Leu589=
ENST00000361715.6:c.1659A>T	ENSP00000355311.2:p.Leu553=
ENST00000361828.6:c.1656A>T	ENSP00000354429.2:p.Leu552=
ENST00000361908.7:c.1713A>T	ENSP00000354681.3:p.Leu571=
ENST00000392438.7:c.1602A>T	ENSP00000376233.3:p.Leu534=
ENST00000483516.1:n.100A>T
NM_015560.2:c.1602A>T , LRG_337t1:c.1602A>T	NP_056375.2:p.Leu534=
NM_130831.2:c.1494A>T	NP_570844.1:p.Leu498=
NM_130832.2:c.1548A>T	NP_570845.1:p.Leu516=
NM_130833.2:c.1605A>T	NP_570846.1:p.Leu535=
NM_130834.2:c.1656A>T	NP_570847.2:p.Leu552=
NM_130835.2:c.1659A>T	NP_570848.1:p.Leu553=
NM_130836.2:c.1713A>T	NP_570849.2:p.Leu571=
NM_130837.2:c.1767A>T , LRG_337t2:c.1767A>T	NP_570850.2:p.Leu589=
XM_011512863.1:c.1767A>T	XP_011511165.1:p.Leu589=
XM_011512864.1:c.1713A>T	XP_011511166.1:p.Leu571=
XM_011512865.1:c.1656A>T	XP_011511167.1:p.Leu552=
XM_011512866.1:c.1605A>T	XP_011511168.1:p.Leu535=
XM_011512867.1:c.1602A>T	XP_011511169.1:p.Leu534=
XM_011512868.1:c.1494A>T	XP_011511170.1:p.Leu498=
XM_011512869.1:c.1767A>T	XP_011511171.1:p.Leu589=
NM_001354663.1:c.1233A>T	NP_001341592.1:p.Leu411=
NM_001354664.1:c.1230A>T	NP_001341593.1:p.Leu410=
XR_001740158.2:n.1996A>T
XR_001740159.2:n.1831A>T
NM_001354663.2:c.1233A>T	NP_001341592.1:p.Leu411=
NM_001354664.2:c.1230A>T	NP_001341593.1:p.Leu410=
NM_130831.3:c.1494A>T	NP_570844.1:p.Leu498=
NM_130832.3:c.1548A>T	NP_570845.1:p.Leu516=
NM_130834.3:c.1656A>T	NP_570847.2:p.Leu552=
NM_130836.3:c.1713A>T	NP_570849.2:p.Leu571=
NM_015560.3:c.1602A>T	NP_056375.2:p.Leu534=
NM_130833.3:c.1605A>T	NP_570846.1:p.Leu535=
NM_130835.3:c.1659A>T	NP_570848.1:p.Leu553=
NM_130837.3:c.1767A>T MANE Select	NP_570850.2:p.Leu589=