Canonical Allele Identifier: CA292630

Gene: OPA1

Linked Data

• ClinVar Variation Id: 138570
• ClinVar RCV Id: RCV000127284 ; RCV000676701 ; RCV001146348
• dbSNP Id: rs144898877
• ExAC: 3:193384966 A / G
• gnomAD v2: 3-193384966-A-G
• gnomAD v3: 3-193667177-A-G
• gnomAD v4: 3-193667177-A-G
• MyVariant Identifiers: chr3:g.193384966A>G (hg19) ; chr3:g.193667177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193667177A>G , CM000665.2:g.193667177A>G	GRCh38
NC_000003.11:g.193384966A>G , CM000665.1:g.193384966A>G	GRCh37
NC_000003.10:g.194867660A>G	NCBI36
NG_011605.1:g.79034A>G , LRG_337:g.79034A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2880A>G MANE Select	ENSP00000355324.2:p.Arg960=
ENST00000361828.7:c.2715A>G	ENSP00000354429.3:p.Arg905=
ENST00000361908.8:c.2826A>G	ENSP00000354681.3:p.Arg942=
ENST00000392436.7:c.2715A>G	ENSP00000376231.3:p.Arg905=
ENST00000392437.6:c.2769A>G	ENSP00000376232.2:p.Arg923=
ENST00000642289.1:c.2654A>G
ENST00000642445.1:c.2715A>G	ENSP00000495535.1:p.Arg905=
ENST00000642593.1:c.*940A>G	ENSP00000494273.1:n.*940A>G
ENST00000643329.1:c.2397A>G	ENSP00000493673.1:p.Arg799=
ENST00000643737.1:c.*2796A>G	ENSP00000494210.1:n.*2796A>G
ENST00000644595.1:c.2715A>G	ENSP00000494121.1:p.Arg905=
ENST00000644629.1:c.2302A>G
ENST00000644841.1:c.*1199A>G	ENSP00000493988.1:n.*1199A>G
ENST00000644959.1:c.2709A>G
ENST00000645553.1:c.2730A>G	ENSP00000494725.1:p.Arg910=
ENST00000646085.1:c.*2193A>G	ENSP00000494509.1:n.*2193A>G
ENST00000646277.1:c.*1316A>G	ENSP00000495289.1:n.*1316A>G
ENST00000646544.1:c.1703A>G
ENST00000646699.1:c.2654A>G
ENST00000646793.1:c.2607A>G	ENSP00000494512.1:p.Arg869=
ENST00000361150.6:c.2718A>G	ENSP00000354781.2:p.Arg906=
ENST00000361510.6:c.2880A>G	ENSP00000355324.2:p.Arg960=
ENST00000361715.6:c.2772A>G	ENSP00000355311.2:p.Arg924=
ENST00000361828.6:c.2769A>G	ENSP00000354429.2:p.Arg923=
ENST00000361908.7:c.2826A>G	ENSP00000354681.3:p.Arg942=
ENST00000392438.7:c.2715A>G	ENSP00000376233.3:p.Arg905=
ENST00000429164.1:c.2A>G
ENST00000445863.1:c.291A>G	ENSP00000398358.1:p.Arg97=
NM_015560.2:c.2715A>G , LRG_337t1:c.2715A>G	NP_056375.2:p.Arg905=
NM_130831.2:c.2607A>G	NP_570844.1:p.Arg869=
NM_130832.2:c.2661A>G	NP_570845.1:p.Arg887=
NM_130833.2:c.2718A>G	NP_570846.1:p.Arg906=
NM_130834.2:c.2769A>G	NP_570847.2:p.Arg923=
NM_130835.2:c.2772A>G	NP_570848.1:p.Arg924=
NM_130836.2:c.2826A>G	NP_570849.2:p.Arg942=
NM_130837.2:c.2880A>G , LRG_337t2:c.2880A>G	NP_570850.2:p.Arg960=
XM_011512863.1:c.2880A>G	XP_011511165.1:p.Arg960=
XM_011512864.1:c.2826A>G	XP_011511166.1:p.Arg942=
XM_011512865.1:c.2769A>G	XP_011511167.1:p.Arg923=
XM_011512866.1:c.2718A>G	XP_011511168.1:p.Arg906=
XM_011512867.1:c.2715A>G	XP_011511169.1:p.Arg905=
XM_011512868.1:c.2607A>G	XP_011511170.1:p.Arg869=
XR_924835.1:n.582+1743T>C
NM_001354663.1:c.2346A>G	NP_001341592.1:p.Arg782=
NM_001354664.1:c.2343A>G	NP_001341593.1:p.Arg781=
XR_001740158.2:n.3134A>G
XR_001740159.2:n.2969A>G
XR_001741072.1:n.600+1743T>C
XR_001741074.1:n.475+3631T>C
XR_924835.2:n.600+1743T>C
NM_001354663.2:c.2346A>G	NP_001341592.1:p.Arg782=
NM_001354664.2:c.2343A>G	NP_001341593.1:p.Arg781=
NM_130831.3:c.2607A>G	NP_570844.1:p.Arg869=
NM_130832.3:c.2661A>G	NP_570845.1:p.Arg887=
NM_130834.3:c.2769A>G	NP_570847.2:p.Arg923=
NM_130836.3:c.2826A>G	NP_570849.2:p.Arg942=
NM_015560.3:c.2715A>G	NP_056375.2:p.Arg905=
NM_130833.3:c.2718A>G	NP_570846.1:p.Arg906=
NM_130835.3:c.2772A>G	NP_570848.1:p.Arg924=
NM_130837.3:c.2880A>G MANE Select	NP_570850.2:p.Arg960=