Canonical Allele Identifier: CA355797901

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193385064A>T (hg19) ; chr3:g.193667275A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193667275A>T , CM000665.2:g.193667275A>T	GRCh38
NC_000003.11:g.193385064A>T , CM000665.1:g.193385064A>T	GRCh37
NC_000003.10:g.194867758A>T	NCBI36
NG_011605.1:g.79132A>T , LRG_337:g.79132A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2978A>T MANE Select	ENSP00000355324.2:p.Asp993Val
ENST00000361828.7:c.2813A>T	ENSP00000354429.3:p.Asp938Val
ENST00000361908.8:c.2924A>T	ENSP00000354681.3:p.Asp975Val
ENST00000392436.7:c.2813A>T	ENSP00000376231.3:p.Asp938Val
ENST00000392437.6:c.2867A>T	ENSP00000376232.2:p.Asp956Val
ENST00000642289.1:c.2752A>T
ENST00000642445.1:c.2813A>T	ENSP00000495535.1:p.Asp938Val
ENST00000642593.1:c.*1038A>T	ENSP00000494273.1:n.*1038A>T
ENST00000643329.1:c.2495A>T	ENSP00000493673.1:p.Asp832Val
ENST00000643737.1:c.*2894A>T	ENSP00000494210.1:n.*2894A>T
ENST00000644595.1:c.2813A>T	ENSP00000494121.1:p.Asp938Val
ENST00000644629.1:c.2400A>T
ENST00000644841.1:c.*1297A>T	ENSP00000493988.1:n.*1297A>T
ENST00000644959.1:c.2807A>T
ENST00000645553.1:c.2828A>T	ENSP00000494725.1:p.Asp943Val
ENST00000646085.1:c.*2291A>T	ENSP00000494509.1:n.*2291A>T
ENST00000646277.1:c.*1414A>T	ENSP00000495289.1:n.*1414A>T
ENST00000646544.1:c.1801A>T
ENST00000646699.1:c.2752A>T
ENST00000646793.1:c.2705A>T	ENSP00000494512.1:p.Asp902Val
ENST00000361150.6:c.2816A>T	ENSP00000354781.2:p.Asp939Val
ENST00000361510.6:c.2978A>T	ENSP00000355324.2:p.Asp993Val
ENST00000361715.6:c.2870A>T	ENSP00000355311.2:p.Asp957Val
ENST00000361828.6:c.2867A>T	ENSP00000354429.2:p.Asp956Val
ENST00000361908.7:c.2924A>T	ENSP00000354681.3:p.Asp975Val
ENST00000392438.7:c.2813A>T	ENSP00000376233.3:p.Asp938Val
ENST00000429164.1:c.100A>T
ENST00000445863.1:c.389A>T	ENSP00000398358.1:p.Asp130Val
NM_015560.2:c.2813A>T , LRG_337t1:c.2813A>T	NP_056375.2:p.Asp938Val
NM_130831.2:c.2705A>T	NP_570844.1:p.Asp902Val
NM_130832.2:c.2759A>T	NP_570845.1:p.Asp920Val
NM_130833.2:c.2816A>T	NP_570846.1:p.Asp939Val
NM_130834.2:c.2867A>T	NP_570847.2:p.Asp956Val
NM_130835.2:c.2870A>T	NP_570848.1:p.Asp957Val
NM_130836.2:c.2924A>T	NP_570849.2:p.Asp975Val
NM_130837.2:c.2978A>T , LRG_337t2:c.2978A>T	NP_570850.2:p.Asp993Val
XM_011512863.1:c.2978A>T	XP_011511165.1:p.Asp993Val
XM_011512864.1:c.2924A>T	XP_011511166.1:p.Asp975Val
XM_011512865.1:c.2867A>T	XP_011511167.1:p.Asp956Val
XM_011512866.1:c.2816A>T	XP_011511168.1:p.Asp939Val
XM_011512867.1:c.2813A>T	XP_011511169.1:p.Asp938Val
XM_011512868.1:c.2705A>T	XP_011511170.1:p.Asp902Val
XR_924835.1:n.582+1645T>A
NM_001354663.1:c.2444A>T	NP_001341592.1:p.Asp815Val
NM_001354664.1:c.2441A>T	NP_001341593.1:p.Asp814Val
XR_001740158.2:n.3232A>T
XR_001740159.2:n.3067A>T
XR_001741072.1:n.600+1645T>A
XR_001741074.1:n.475+3533T>A
XR_924835.2:n.600+1645T>A
NM_001354663.2:c.2444A>T	NP_001341592.1:p.Asp815Val
NM_001354664.2:c.2441A>T	NP_001341593.1:p.Asp814Val
NM_130831.3:c.2705A>T	NP_570844.1:p.Asp902Val
NM_130832.3:c.2759A>T	NP_570845.1:p.Asp920Val
NM_130834.3:c.2867A>T	NP_570847.2:p.Asp956Val
NM_130836.3:c.2924A>T	NP_570849.2:p.Asp975Val
NM_015560.3:c.2813A>T	NP_056375.2:p.Asp938Val
NM_130833.3:c.2816A>T	NP_570846.1:p.Asp939Val
NM_130835.3:c.2870A>T	NP_570848.1:p.Asp957Val
NM_130837.3:c.2978A>T MANE Select	NP_570850.2:p.Asp993Val