Canonical Allele Identifier: CA355789261

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193361199G>C (hg19) ; chr3:g.193643410G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193643410G>C , CM000665.2:g.193643410G>C	GRCh38
NC_000003.11:g.193361199G>C , CM000665.1:g.193361199G>C	GRCh37
NC_000003.10:g.194843893G>C	NCBI36
NG_011605.1:g.55267G>C , LRG_337:g.55267G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1343G>C MANE Select	ENSP00000355324.2:p.Arg448Thr
ENST00000361828.7:c.1178G>C	ENSP00000354429.3:p.Arg393Thr
ENST00000361908.8:c.1289G>C	ENSP00000354681.3:p.Arg430Thr
ENST00000392436.7:c.1178G>C	ENSP00000376231.3:p.Arg393Thr
ENST00000392437.6:c.1232G>C	ENSP00000376232.2:p.Arg411Thr
ENST00000642289.1:c.1117G>C
ENST00000642445.1:c.1178G>C	ENSP00000495535.1:p.Arg393Thr
ENST00000642593.1:c.1178G>C	ENSP00000494273.1:p.Arg393Thr
ENST00000643329.1:c.860G>C	ENSP00000493673.1:p.Arg287Thr
ENST00000643737.1:c.*1259G>C	ENSP00000494210.1:n.*1259G>C
ENST00000644595.1:c.1178G>C	ENSP00000494121.1:p.Arg393Thr
ENST00000644629.1:c.838G>C
ENST00000644841.1:c.806G>C	ENSP00000493988.1:p.Arg269Thr
ENST00000644959.1:c.1147G>C
ENST00000645553.1:c.1193G>C	ENSP00000494725.1:p.Arg398Thr
ENST00000646085.1:c.*656G>C	ENSP00000494509.1:n.*656G>C
ENST00000646277.1:c.1343G>C	ENSP00000495289.1:p.Arg448Thr
ENST00000646544.1:c.166G>C
ENST00000646699.1:c.1117G>C
ENST00000646793.1:c.1070G>C	ENSP00000494512.1:p.Arg357Thr
ENST00000361150.6:c.1181G>C	ENSP00000354781.2:p.Arg394Thr
ENST00000361510.6:c.1343G>C	ENSP00000355324.2:p.Arg448Thr
ENST00000361715.6:c.1235G>C	ENSP00000355311.2:p.Arg412Thr
ENST00000361828.6:c.1232G>C	ENSP00000354429.2:p.Arg411Thr
ENST00000361908.7:c.1289G>C	ENSP00000354681.3:p.Arg430Thr
ENST00000392438.7:c.1178G>C	ENSP00000376233.3:p.Arg393Thr
ENST00000475899.1:n.374G>C
NM_015560.2:c.1178G>C , LRG_337t1:c.1178G>C	NP_056375.2:p.Arg393Thr
NM_130831.2:c.1070G>C	NP_570844.1:p.Arg357Thr
NM_130832.2:c.1124G>C	NP_570845.1:p.Arg375Thr
NM_130833.2:c.1181G>C	NP_570846.1:p.Arg394Thr
NM_130834.2:c.1232G>C	NP_570847.2:p.Arg411Thr
NM_130835.2:c.1235G>C	NP_570848.1:p.Arg412Thr
NM_130836.2:c.1289G>C	NP_570849.2:p.Arg430Thr
NM_130837.2:c.1343G>C , LRG_337t2:c.1343G>C	NP_570850.2:p.Arg448Thr
XM_011512863.1:c.1343G>C	XP_011511165.1:p.Arg448Thr
XM_011512864.1:c.1289G>C	XP_011511166.1:p.Arg430Thr
XM_011512865.1:c.1232G>C	XP_011511167.1:p.Arg411Thr
XM_011512866.1:c.1181G>C	XP_011511168.1:p.Arg394Thr
XM_011512867.1:c.1178G>C	XP_011511169.1:p.Arg393Thr
XM_011512868.1:c.1070G>C	XP_011511170.1:p.Arg357Thr
XM_011512869.1:c.1343G>C	XP_011511171.1:p.Arg448Thr
NM_001354663.1:c.809G>C	NP_001341592.1:p.Arg270Thr
NM_001354664.1:c.806G>C	NP_001341593.1:p.Arg269Thr
XR_001740158.2:n.1572G>C
XR_001740159.2:n.1407G>C
NM_001354663.2:c.809G>C	NP_001341592.1:p.Arg270Thr
NM_001354664.2:c.806G>C	NP_001341593.1:p.Arg269Thr
NM_130831.3:c.1070G>C	NP_570844.1:p.Arg357Thr
NM_130832.3:c.1124G>C	NP_570845.1:p.Arg375Thr
NM_130834.3:c.1232G>C	NP_570847.2:p.Arg411Thr
NM_130836.3:c.1289G>C	NP_570849.2:p.Arg430Thr
NM_015560.3:c.1178G>C	NP_056375.2:p.Arg393Thr
NM_130833.3:c.1181G>C	NP_570846.1:p.Arg394Thr
NM_130835.3:c.1235G>C	NP_570848.1:p.Arg412Thr
NM_130837.3:c.1343G>C MANE Select	NP_570850.2:p.Arg448Thr