Canonical Allele Identifier: CA355792934

Gene: OPA1

Linked Data

• ClinVar Variation Id: 447899
• ClinVar RCV Id: RCV000517407
• dbSNP Id: rs1553785338
• MyVariant Identifiers: chr3:g.193377329G>A (hg19) ; chr3:g.193659540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659540G>A , CM000665.2:g.193659540G>A	GRCh38
NC_000003.11:g.193377329G>A , CM000665.1:g.193377329G>A	GRCh37
NC_000003.10:g.194860023G>A	NCBI36
NG_011605.1:g.71397G>A , LRG_337:g.71397G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2499G>A MANE Select	ENSP00000355324.2:p.Trp833Ter
ENST00000361828.7:c.2334G>A	ENSP00000354429.3:p.Trp778Ter
ENST00000361908.8:c.2445G>A	ENSP00000354681.3:p.Trp815Ter
ENST00000392436.7:c.2334G>A	ENSP00000376231.3:p.Trp778Ter
ENST00000392437.6:c.2388G>A	ENSP00000376232.2:p.Trp796Ter
ENST00000642289.1:c.2273G>A
ENST00000642445.1:c.2334G>A	ENSP00000495535.1:p.Trp778Ter
ENST00000642593.1:c.*559G>A	ENSP00000494273.1:n.*559G>A
ENST00000643329.1:c.2016G>A	ENSP00000493673.1:p.Trp672Ter
ENST00000643737.1:c.*2415G>A	ENSP00000494210.1:n.*2415G>A
ENST00000644595.1:c.2334G>A	ENSP00000494121.1:p.Trp778Ter
ENST00000644629.1:c.1921G>A
ENST00000644841.1:c.*818G>A	ENSP00000493988.1:n.*818G>A
ENST00000644959.1:c.2328G>A
ENST00000645553.1:c.2349G>A	ENSP00000494725.1:p.Trp783Ter
ENST00000646085.1:c.*1812G>A	ENSP00000494509.1:n.*1812G>A
ENST00000646277.1:c.*935G>A	ENSP00000495289.1:n.*935G>A
ENST00000646544.1:c.1322G>A
ENST00000646699.1:c.2273G>A
ENST00000646793.1:c.2226G>A	ENSP00000494512.1:p.Trp742Ter
ENST00000361150.6:c.2337G>A	ENSP00000354781.2:p.Trp779Ter
ENST00000361510.6:c.2499G>A	ENSP00000355324.2:p.Trp833Ter
ENST00000361715.6:c.2391G>A	ENSP00000355311.2:p.Trp797Ter
ENST00000361828.6:c.2388G>A	ENSP00000354429.2:p.Trp796Ter
ENST00000361908.7:c.2445G>A	ENSP00000354681.3:p.Trp815Ter
ENST00000392438.7:c.2334G>A	ENSP00000376233.3:p.Trp778Ter
NM_015560.2:c.2334G>A , LRG_337t1:c.2334G>A	NP_056375.2:p.Trp778Ter
NM_130831.2:c.2226G>A	NP_570844.1:p.Trp742Ter
NM_130832.2:c.2280G>A	NP_570845.1:p.Trp760Ter
NM_130833.2:c.2337G>A	NP_570846.1:p.Trp779Ter
NM_130834.2:c.2388G>A	NP_570847.2:p.Trp796Ter
NM_130835.2:c.2391G>A	NP_570848.1:p.Trp797Ter
NM_130836.2:c.2445G>A	NP_570849.2:p.Trp815Ter
NM_130837.2:c.2499G>A , LRG_337t2:c.2499G>A	NP_570850.2:p.Trp833Ter
XM_011512863.1:c.2499G>A	XP_011511165.1:p.Trp833Ter
XM_011512864.1:c.2445G>A	XP_011511166.1:p.Trp815Ter
XM_011512865.1:c.2388G>A	XP_011511167.1:p.Trp796Ter
XM_011512866.1:c.2337G>A	XP_011511168.1:p.Trp779Ter
XM_011512867.1:c.2334G>A	XP_011511169.1:p.Trp778Ter
XM_011512868.1:c.2226G>A	XP_011511170.1:p.Trp742Ter
XR_924835.1:n.582+9380C>T
NM_001354663.1:c.1965G>A	NP_001341592.1:p.Trp655Ter
NM_001354664.1:c.1962G>A	NP_001341593.1:p.Trp654Ter
XR_001740158.2:n.2753G>A
XR_001740159.2:n.2588G>A
XR_001741074.1:n.475+11268C>T
XR_924835.2:n.600+9380C>T
NM_001354663.2:c.1965G>A	NP_001341592.1:p.Trp655Ter
NM_001354664.2:c.1962G>A	NP_001341593.1:p.Trp654Ter
NM_130831.3:c.2226G>A	NP_570844.1:p.Trp742Ter
NM_130832.3:c.2280G>A	NP_570845.1:p.Trp760Ter
NM_130834.3:c.2388G>A	NP_570847.2:p.Trp796Ter
NM_130836.3:c.2445G>A	NP_570849.2:p.Trp815Ter
NM_015560.3:c.2334G>A	NP_056375.2:p.Trp778Ter
NM_130833.3:c.2337G>A	NP_570846.1:p.Trp779Ter
NM_130835.3:c.2391G>A	NP_570848.1:p.Trp797Ter
NM_130837.3:c.2499G>A MANE Select	NP_570850.2:p.Trp833Ter