Canonical Allele Identifier: CA355797491

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193385016A>T (hg19) ; chr3:g.193667227A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193667227A>T , CM000665.2:g.193667227A>T	GRCh38
NC_000003.11:g.193385016A>T , CM000665.1:g.193385016A>T	GRCh37
NC_000003.10:g.194867710A>T	NCBI36
NG_011605.1:g.79084A>T , LRG_337:g.79084A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2930A>T MANE Select	ENSP00000355324.2:p.Glu977Val
ENST00000361828.7:c.2765A>T	ENSP00000354429.3:p.Glu922Val
ENST00000361908.8:c.2876A>T	ENSP00000354681.3:p.Glu959Val
ENST00000392436.7:c.2765A>T	ENSP00000376231.3:p.Glu922Val
ENST00000392437.6:c.2819A>T	ENSP00000376232.2:p.Glu940Val
ENST00000642289.1:c.2704A>T
ENST00000642445.1:c.2765A>T	ENSP00000495535.1:p.Glu922Val
ENST00000642593.1:c.*990A>T	ENSP00000494273.1:n.*990A>T
ENST00000643329.1:c.2447A>T	ENSP00000493673.1:p.Glu816Val
ENST00000643737.1:c.*2846A>T	ENSP00000494210.1:n.*2846A>T
ENST00000644595.1:c.2765A>T	ENSP00000494121.1:p.Glu922Val
ENST00000644629.1:c.2352A>T
ENST00000644841.1:c.*1249A>T	ENSP00000493988.1:n.*1249A>T
ENST00000644959.1:c.2759A>T
ENST00000645553.1:c.2780A>T	ENSP00000494725.1:p.Glu927Val
ENST00000646085.1:c.*2243A>T	ENSP00000494509.1:n.*2243A>T
ENST00000646277.1:c.*1366A>T	ENSP00000495289.1:n.*1366A>T
ENST00000646544.1:c.1753A>T
ENST00000646699.1:c.2704A>T
ENST00000646793.1:c.2657A>T	ENSP00000494512.1:p.Glu886Val
ENST00000361150.6:c.2768A>T	ENSP00000354781.2:p.Glu923Val
ENST00000361510.6:c.2930A>T	ENSP00000355324.2:p.Glu977Val
ENST00000361715.6:c.2822A>T	ENSP00000355311.2:p.Glu941Val
ENST00000361828.6:c.2819A>T	ENSP00000354429.2:p.Glu940Val
ENST00000361908.7:c.2876A>T	ENSP00000354681.3:p.Glu959Val
ENST00000392438.7:c.2765A>T	ENSP00000376233.3:p.Glu922Val
ENST00000429164.1:c.52A>T
ENST00000445863.1:c.341A>T	ENSP00000398358.1:p.Glu114Val
NM_015560.2:c.2765A>T , LRG_337t1:c.2765A>T	NP_056375.2:p.Glu922Val
NM_130831.2:c.2657A>T	NP_570844.1:p.Glu886Val
NM_130832.2:c.2711A>T	NP_570845.1:p.Glu904Val
NM_130833.2:c.2768A>T	NP_570846.1:p.Glu923Val
NM_130834.2:c.2819A>T	NP_570847.2:p.Glu940Val
NM_130835.2:c.2822A>T	NP_570848.1:p.Glu941Val
NM_130836.2:c.2876A>T	NP_570849.2:p.Glu959Val
NM_130837.2:c.2930A>T , LRG_337t2:c.2930A>T	NP_570850.2:p.Glu977Val
XM_011512863.1:c.2930A>T	XP_011511165.1:p.Glu977Val
XM_011512864.1:c.2876A>T	XP_011511166.1:p.Glu959Val
XM_011512865.1:c.2819A>T	XP_011511167.1:p.Glu940Val
XM_011512866.1:c.2768A>T	XP_011511168.1:p.Glu923Val
XM_011512867.1:c.2765A>T	XP_011511169.1:p.Glu922Val
XM_011512868.1:c.2657A>T	XP_011511170.1:p.Glu886Val
XR_924835.1:n.582+1693T>A
NM_001354663.1:c.2396A>T	NP_001341592.1:p.Glu799Val
NM_001354664.1:c.2393A>T	NP_001341593.1:p.Glu798Val
XR_001740158.2:n.3184A>T
XR_001740159.2:n.3019A>T
XR_001741072.1:n.600+1693T>A
XR_001741074.1:n.475+3581T>A
XR_924835.2:n.600+1693T>A
NM_001354663.2:c.2396A>T	NP_001341592.1:p.Glu799Val
NM_001354664.2:c.2393A>T	NP_001341593.1:p.Glu798Val
NM_130831.3:c.2657A>T	NP_570844.1:p.Glu886Val
NM_130832.3:c.2711A>T	NP_570845.1:p.Glu904Val
NM_130834.3:c.2819A>T	NP_570847.2:p.Glu940Val
NM_130836.3:c.2876A>T	NP_570849.2:p.Glu959Val
NM_015560.3:c.2765A>T	NP_056375.2:p.Glu922Val
NM_130833.3:c.2768A>T	NP_570846.1:p.Glu923Val
NM_130835.3:c.2822A>T	NP_570848.1:p.Glu941Val
NM_130837.3:c.2930A>T MANE Select	NP_570850.2:p.Glu977Val