Canonical Allele Identifier: CA355792817

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377280C>T (hg19) ; chr3:g.193659491C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659491C>T , CM000665.2:g.193659491C>T	GRCh38
NC_000003.11:g.193377280C>T , CM000665.1:g.193377280C>T	GRCh37
NC_000003.10:g.194859974C>T	NCBI36
NG_011605.1:g.71348C>T , LRG_337:g.71348C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2450C>T MANE Select	ENSP00000355324.2:p.Ala817Val
ENST00000361828.7:c.2285C>T	ENSP00000354429.3:p.Ala762Val
ENST00000361908.8:c.2396C>T	ENSP00000354681.3:p.Ala799Val
ENST00000392436.7:c.2285C>T	ENSP00000376231.3:p.Ala762Val
ENST00000392437.6:c.2339C>T	ENSP00000376232.2:p.Ala780Val
ENST00000642289.1:c.2224C>T
ENST00000642445.1:c.2285C>T	ENSP00000495535.1:p.Ala762Val
ENST00000642593.1:c.*510C>T	ENSP00000494273.1:n.*510C>T
ENST00000643329.1:c.1967C>T	ENSP00000493673.1:p.Ala656Val
ENST00000643737.1:c.*2366C>T	ENSP00000494210.1:n.*2366C>T
ENST00000644595.1:c.2285C>T	ENSP00000494121.1:p.Ala762Val
ENST00000644629.1:c.1872C>T
ENST00000644841.1:c.*769C>T	ENSP00000493988.1:n.*769C>T
ENST00000644959.1:c.2279C>T
ENST00000645553.1:c.2300C>T	ENSP00000494725.1:p.Ala767Val
ENST00000646085.1:c.*1763C>T	ENSP00000494509.1:n.*1763C>T
ENST00000646277.1:c.*886C>T	ENSP00000495289.1:n.*886C>T
ENST00000646544.1:c.1273C>T
ENST00000646699.1:c.2224C>T
ENST00000646793.1:c.2177C>T	ENSP00000494512.1:p.Ala726Val
ENST00000361150.6:c.2288C>T	ENSP00000354781.2:p.Ala763Val
ENST00000361510.6:c.2450C>T	ENSP00000355324.2:p.Ala817Val
ENST00000361715.6:c.2342C>T	ENSP00000355311.2:p.Ala781Val
ENST00000361828.6:c.2339C>T	ENSP00000354429.2:p.Ala780Val
ENST00000361908.7:c.2396C>T	ENSP00000354681.3:p.Ala799Val
ENST00000392438.7:c.2285C>T	ENSP00000376233.3:p.Ala762Val
ENST00000482865.1:n.544C>T
NM_015560.2:c.2285C>T , LRG_337t1:c.2285C>T	NP_056375.2:p.Ala762Val
NM_130831.2:c.2177C>T	NP_570844.1:p.Ala726Val
NM_130832.2:c.2231C>T	NP_570845.1:p.Ala744Val
NM_130833.2:c.2288C>T	NP_570846.1:p.Ala763Val
NM_130834.2:c.2339C>T	NP_570847.2:p.Ala780Val
NM_130835.2:c.2342C>T	NP_570848.1:p.Ala781Val
NM_130836.2:c.2396C>T	NP_570849.2:p.Ala799Val
NM_130837.2:c.2450C>T , LRG_337t2:c.2450C>T	NP_570850.2:p.Ala817Val
XM_011512863.1:c.2450C>T	XP_011511165.1:p.Ala817Val
XM_011512864.1:c.2396C>T	XP_011511166.1:p.Ala799Val
XM_011512865.1:c.2339C>T	XP_011511167.1:p.Ala780Val
XM_011512866.1:c.2288C>T	XP_011511168.1:p.Ala763Val
XM_011512867.1:c.2285C>T	XP_011511169.1:p.Ala762Val
XM_011512868.1:c.2177C>T	XP_011511170.1:p.Ala726Val
XR_924835.1:n.582+9429G>A
NM_001354663.1:c.1916C>T	NP_001341592.1:p.Ala639Val
NM_001354664.1:c.1913C>T	NP_001341593.1:p.Ala638Val
XR_001740158.2:n.2704C>T
XR_001740159.2:n.2539C>T
XR_001741074.1:n.475+11317G>A
XR_924835.2:n.600+9429G>A
NM_001354663.2:c.1916C>T	NP_001341592.1:p.Ala639Val
NM_001354664.2:c.1913C>T	NP_001341593.1:p.Ala638Val
NM_130831.3:c.2177C>T	NP_570844.1:p.Ala726Val
NM_130832.3:c.2231C>T	NP_570845.1:p.Ala744Val
NM_130834.3:c.2339C>T	NP_570847.2:p.Ala780Val
NM_130836.3:c.2396C>T	NP_570849.2:p.Ala799Val
NM_015560.3:c.2285C>T	NP_056375.2:p.Ala762Val
NM_130833.3:c.2288C>T	NP_570846.1:p.Ala763Val
NM_130835.3:c.2342C>T	NP_570848.1:p.Ala781Val
NM_130837.3:c.2450C>T MANE Select	NP_570850.2:p.Ala817Val