Canonical Allele Identifier: CA1430270656

Gene: OPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662893T= , CM000665.2:g.193662893T=	GRCh38
NC_000003.11:g.193380682T= , CM000665.1:g.193380682T=	GRCh37
NC_000003.10:g.194863376T=	NCBI36
NG_011605.1:g.74750T= , LRG_337:g.74750T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2592T= MANE Select	ENSP00000355324.2:p.Leu864=
ENST00000361828.7:c.2427T=	ENSP00000354429.3:p.Leu809=
ENST00000361908.8:c.2538T=	ENSP00000354681.3:p.Leu846=
ENST00000392436.7:c.2427T=	ENSP00000376231.3:p.Leu809=
ENST00000392437.6:c.2481T=	ENSP00000376232.2:p.Leu827=
ENST00000642289.1:c.2366T=
ENST00000642445.1:c.2427T=	ENSP00000495535.1:p.Leu809=
ENST00000642593.1:c.*652T=	ENSP00000494273.1:n.*652T=
ENST00000643329.1:c.2109T=	ENSP00000493673.1:p.Leu703=
ENST00000643737.1:c.*2508T=	ENSP00000494210.1:n.*2508T=
ENST00000644595.1:c.2427T=	ENSP00000494121.1:p.Leu809=
ENST00000644629.1:c.2014T=
ENST00000644841.1:c.*911T=	ENSP00000493988.1:n.*911T=
ENST00000644959.1:c.2421T=
ENST00000645553.1:c.2442T=	ENSP00000494725.1:p.Leu814=
ENST00000646085.1:c.*1905T=	ENSP00000494509.1:n.*1905T=
ENST00000646277.1:c.*1028T=	ENSP00000495289.1:n.*1028T=
ENST00000646544.1:c.1415T=
ENST00000646699.1:c.2366T=
ENST00000646793.1:c.2319T=	ENSP00000494512.1:p.Leu773=
ENST00000361150.6:c.2430T=	ENSP00000354781.2:p.Leu810=
ENST00000361510.6:c.2592T=	ENSP00000355324.2:p.Leu864=
ENST00000361715.6:c.2484T=	ENSP00000355311.2:p.Leu828=
ENST00000361828.6:c.2481T=	ENSP00000354429.2:p.Leu827=
ENST00000361908.7:c.2538T=	ENSP00000354681.3:p.Leu846=
ENST00000392438.7:c.2427T=	ENSP00000376233.3:p.Leu809=
ENST00000445863.1:c.3T=	ENSP00000398358.1:p.Leu1=
NM_015560.2:c.2427T= , LRG_337t1:c.2427T=	NP_056375.2:p.Leu809=
NM_130831.2:c.2319T=	NP_570844.1:p.Leu773=
NM_130832.2:c.2373T=	NP_570845.1:p.Leu791=
NM_130833.2:c.2430T=	NP_570846.1:p.Leu810=
NM_130834.2:c.2481T=	NP_570847.2:p.Leu827=
NM_130835.2:c.2484T=	NP_570848.1:p.Leu828=
NM_130836.2:c.2538T=	NP_570849.2:p.Leu846=
NM_130837.2:c.2592T= , LRG_337t2:c.2592T=	NP_570850.2:p.Leu864=
XM_011512863.1:c.2592T=	XP_011511165.1:p.Leu864=
XM_011512864.1:c.2538T=	XP_011511166.1:p.Leu846=
XM_011512865.1:c.2481T=	XP_011511167.1:p.Leu827=
XM_011512866.1:c.2430T=	XP_011511168.1:p.Leu810=
XM_011512867.1:c.2427T=	XP_011511169.1:p.Leu809=
XM_011512868.1:c.2319T=	XP_011511170.1:p.Leu773=
XR_924835.1:n.582+6027A=
NM_001354663.1:c.2058T=	NP_001341592.1:p.Leu686=
NM_001354664.1:c.2055T=	NP_001341593.1:p.Leu685=
XR_001740158.2:n.2846T=
XR_001740159.2:n.2681T=
XR_001741072.1:n.601-2808A=
XR_001741074.1:n.475+7915A=
XR_924835.2:n.600+6027A=
NM_001354663.2:c.2058T=	NP_001341592.1:p.Leu686=
NM_001354664.2:c.2055T=	NP_001341593.1:p.Leu685=
NM_130831.3:c.2319T=	NP_570844.1:p.Leu773=
NM_130832.3:c.2373T=	NP_570845.1:p.Leu791=
NM_130834.3:c.2481T=	NP_570847.2:p.Leu827=
NM_130836.3:c.2538T=	NP_570849.2:p.Leu846=
NM_015560.3:c.2427T=	NP_056375.2:p.Leu809=
NM_130833.3:c.2430T=	NP_570846.1:p.Leu810=
NM_130835.3:c.2484T=	NP_570848.1:p.Leu828=
NM_130837.3:c.2592T= MANE Select	NP_570850.2:p.Leu864=