Canonical Allele Identifier: CA355793255

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193380721A>C (hg19) ; chr3:g.193662932A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662932A>C , CM000665.2:g.193662932A>C	GRCh38
NC_000003.11:g.193380721A>C , CM000665.1:g.193380721A>C	GRCh37
NC_000003.10:g.194863415A>C	NCBI36
NG_011605.1:g.74789A>C , LRG_337:g.74789A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2631A>C MANE Select	ENSP00000355324.2:p.Glu877Asp
ENST00000361828.7:c.2466A>C	ENSP00000354429.3:p.Glu822Asp
ENST00000361908.8:c.2577A>C	ENSP00000354681.3:p.Glu859Asp
ENST00000392436.7:c.2466A>C	ENSP00000376231.3:p.Glu822Asp
ENST00000392437.6:c.2520A>C	ENSP00000376232.2:p.Glu840Asp
ENST00000642289.1:c.2405A>C
ENST00000642445.1:c.2466A>C	ENSP00000495535.1:p.Glu822Asp
ENST00000642593.1:c.*691A>C	ENSP00000494273.1:n.*691A>C
ENST00000643329.1:c.2148A>C	ENSP00000493673.1:p.Glu716Asp
ENST00000643737.1:c.*2547A>C	ENSP00000494210.1:n.*2547A>C
ENST00000644595.1:c.2466A>C	ENSP00000494121.1:p.Glu822Asp
ENST00000644629.1:c.2053A>C
ENST00000644841.1:c.*950A>C	ENSP00000493988.1:n.*950A>C
ENST00000644959.1:c.2460A>C
ENST00000645553.1:c.2481A>C	ENSP00000494725.1:p.Glu827Asp
ENST00000646085.1:c.*1944A>C	ENSP00000494509.1:n.*1944A>C
ENST00000646277.1:c.*1067A>C	ENSP00000495289.1:n.*1067A>C
ENST00000646544.1:c.1454A>C
ENST00000646699.1:c.2405A>C
ENST00000646793.1:c.2358A>C	ENSP00000494512.1:p.Glu786Asp
ENST00000361150.6:c.2469A>C	ENSP00000354781.2:p.Glu823Asp
ENST00000361510.6:c.2631A>C	ENSP00000355324.2:p.Glu877Asp
ENST00000361715.6:c.2523A>C	ENSP00000355311.2:p.Glu841Asp
ENST00000361828.6:c.2520A>C	ENSP00000354429.2:p.Glu840Asp
ENST00000361908.7:c.2577A>C	ENSP00000354681.3:p.Glu859Asp
ENST00000392438.7:c.2466A>C	ENSP00000376233.3:p.Glu822Asp
ENST00000445863.1:c.42A>C	ENSP00000398358.1:p.Glu14Asp
NM_015560.2:c.2466A>C , LRG_337t1:c.2466A>C	NP_056375.2:p.Glu822Asp
NM_130831.2:c.2358A>C	NP_570844.1:p.Glu786Asp
NM_130832.2:c.2412A>C	NP_570845.1:p.Glu804Asp
NM_130833.2:c.2469A>C	NP_570846.1:p.Glu823Asp
NM_130834.2:c.2520A>C	NP_570847.2:p.Glu840Asp
NM_130835.2:c.2523A>C	NP_570848.1:p.Glu841Asp
NM_130836.2:c.2577A>C	NP_570849.2:p.Glu859Asp
NM_130837.2:c.2631A>C , LRG_337t2:c.2631A>C	NP_570850.2:p.Glu877Asp
XM_011512863.1:c.2631A>C	XP_011511165.1:p.Glu877Asp
XM_011512864.1:c.2577A>C	XP_011511166.1:p.Glu859Asp
XM_011512865.1:c.2520A>C	XP_011511167.1:p.Glu840Asp
XM_011512866.1:c.2469A>C	XP_011511168.1:p.Glu823Asp
XM_011512867.1:c.2466A>C	XP_011511169.1:p.Glu822Asp
XM_011512868.1:c.2358A>C	XP_011511170.1:p.Glu786Asp
XR_924835.1:n.582+5988T>G
NM_001354663.1:c.2097A>C	NP_001341592.1:p.Glu699Asp
NM_001354664.1:c.2094A>C	NP_001341593.1:p.Glu698Asp
XR_001740158.2:n.2885A>C
XR_001740159.2:n.2720A>C
XR_001741072.1:n.601-2847T>G
XR_001741074.1:n.475+7876T>G
XR_924835.2:n.600+5988T>G
NM_001354663.2:c.2097A>C	NP_001341592.1:p.Glu699Asp
NM_001354664.2:c.2094A>C	NP_001341593.1:p.Glu698Asp
NM_130831.3:c.2358A>C	NP_570844.1:p.Glu786Asp
NM_130832.3:c.2412A>C	NP_570845.1:p.Glu804Asp
NM_130834.3:c.2520A>C	NP_570847.2:p.Glu840Asp
NM_130836.3:c.2577A>C	NP_570849.2:p.Glu859Asp
NM_015560.3:c.2466A>C	NP_056375.2:p.Glu822Asp
NM_130833.3:c.2469A>C	NP_570846.1:p.Glu823Asp
NM_130835.3:c.2523A>C	NP_570848.1:p.Glu841Asp
NM_130837.3:c.2631A>C MANE Select	NP_570850.2:p.Glu877Asp