Canonical Allele Identifier: CA437435594

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193360616T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193642827T>C , CM000665.2:g.193642827T>C	GRCh38
NC_000003.11:g.193360616T>C , CM000665.1:g.193360616T>C	GRCh37
NC_000003.10:g.194843310T>C	NCBI36
NG_011605.1:g.54684T>C , LRG_337:g.54684T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1212T>C MANE Select	ENSP00000355324.2:p.Asp404=
ENST00000361828.7:c.1047T>C	ENSP00000354429.3:p.Asp349=
ENST00000361908.8:c.1158T>C	ENSP00000354681.3:p.Asp386=
ENST00000392436.7:c.1047T>C	ENSP00000376231.3:p.Asp349=
ENST00000392437.6:c.1101T>C	ENSP00000376232.2:p.Asp367=
ENST00000642289.1:c.1080-546T>C
ENST00000642445.1:c.1047T>C	ENSP00000495535.1:p.Asp349=
ENST00000642593.1:c.1047T>C	ENSP00000494273.1:p.Asp349=
ENST00000643329.1:c.729T>C	ENSP00000493673.1:p.Asp243=
ENST00000643737.1:c.*1128T>C	ENSP00000494210.1:n.*1128T>C
ENST00000644595.1:c.1047T>C	ENSP00000494121.1:p.Asp349=
ENST00000644629.1:c.707T>C
ENST00000644841.1:c.675T>C	ENSP00000493988.1:p.Asp225=
ENST00000644959.1:c.1016T>C
ENST00000645553.1:c.1062T>C	ENSP00000494725.1:p.Asp354=
ENST00000646085.1:c.*525T>C	ENSP00000494509.1:n.*525T>C
ENST00000646277.1:c.1212T>C	ENSP00000495289.1:p.Asp404=
ENST00000646544.1:c.110T>C
ENST00000646699.1:c.1080-546T>C
ENST00000646793.1:c.939T>C	ENSP00000494512.1:p.Asp313=
ENST00000361150.6:c.1050T>C	ENSP00000354781.2:p.Asp350=
ENST00000361510.6:c.1212T>C	ENSP00000355324.2:p.Asp404=
ENST00000361715.6:c.1104T>C	ENSP00000355311.2:p.Asp368=
ENST00000361828.6:c.1101T>C	ENSP00000354429.2:p.Asp367=
ENST00000361908.7:c.1158T>C	ENSP00000354681.3:p.Asp386=
ENST00000392438.7:c.1047T>C	ENSP00000376233.3:p.Asp349=
ENST00000475899.1:n.243T>C
ENST00000497189.5:n.533T>C
NM_015560.2:c.1047T>C , LRG_337t1:c.1047T>C	NP_056375.2:p.Asp349=
NM_130831.2:c.939T>C	NP_570844.1:p.Asp313=
NM_130832.2:c.993T>C	NP_570845.1:p.Asp331=
NM_130833.2:c.1050T>C	NP_570846.1:p.Asp350=
NM_130834.2:c.1101T>C	NP_570847.2:p.Asp367=
NM_130835.2:c.1104T>C	NP_570848.1:p.Asp368=
NM_130836.2:c.1158T>C	NP_570849.2:p.Asp386=
NM_130837.2:c.1212T>C , LRG_337t2:c.1212T>C	NP_570850.2:p.Asp404=
XM_011512863.1:c.1212T>C	XP_011511165.1:p.Asp404=
XM_011512864.1:c.1158T>C	XP_011511166.1:p.Asp386=
XM_011512865.1:c.1101T>C	XP_011511167.1:p.Asp367=
XM_011512866.1:c.1050T>C	XP_011511168.1:p.Asp350=
XM_011512867.1:c.1047T>C	XP_011511169.1:p.Asp349=
XM_011512868.1:c.939T>C	XP_011511170.1:p.Asp313=
XM_011512869.1:c.1212T>C	XP_011511171.1:p.Asp404=
NM_001354663.1:c.678T>C	NP_001341592.1:p.Asp226=
NM_001354664.1:c.675T>C	NP_001341593.1:p.Asp225=
XR_001740158.2:n.1441T>C
XR_001740159.2:n.1276T>C
NM_001354663.2:c.678T>C	NP_001341592.1:p.Asp226=
NM_001354664.2:c.675T>C	NP_001341593.1:p.Asp225=
NM_130831.3:c.939T>C	NP_570844.1:p.Asp313=
NM_130832.3:c.993T>C	NP_570845.1:p.Asp331=
NM_130834.3:c.1101T>C	NP_570847.2:p.Asp367=
NM_130836.3:c.1158T>C	NP_570849.2:p.Asp386=
NM_015560.3:c.1047T>C	NP_056375.2:p.Asp349=
NM_130833.3:c.1050T>C	NP_570846.1:p.Asp350=
NM_130835.3:c.1104T>C	NP_570848.1:p.Asp368=
NM_130837.3:c.1212T>C MANE Select	NP_570850.2:p.Asp404=