Canonical Allele Identifier: CA355790434

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193364895T>G (hg19) ; chr3:g.193647106T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647106T>G , CM000665.2:g.193647106T>G	GRCh38
NC_000003.11:g.193364895T>G , CM000665.1:g.193364895T>G	GRCh37
NC_000003.10:g.194847589T>G	NCBI36
NG_011605.1:g.58963T>G , LRG_337:g.58963T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.1796T>G MANE Select	ENSP00000355324.2:p.Leu599Ter
ENST00000361828.7:c.1631T>G	ENSP00000354429.3:p.Leu544Ter
ENST00000361908.8:c.1742T>G	ENSP00000354681.3:p.Leu581Ter
ENST00000392436.7:c.1631T>G	ENSP00000376231.3:p.Leu544Ter
ENST00000392437.6:c.1685T>G	ENSP00000376232.2:p.Leu562Ter
ENST00000642289.1:c.1570T>G
ENST00000642445.1:c.1631T>G	ENSP00000495535.1:p.Leu544Ter
ENST00000642593.1:c.1631T>G	ENSP00000494273.1:p.Leu544Ter
ENST00000643329.1:c.1313T>G	ENSP00000493673.1:p.Leu438Ter
ENST00000643737.1:c.*1712T>G	ENSP00000494210.1:n.*1712T>G
ENST00000644595.1:c.1631T>G	ENSP00000494121.1:p.Leu544Ter
ENST00000644629.1:c.1218T>G
ENST00000644841.1:c.*115T>G	ENSP00000493988.1:n.*115T>G
ENST00000644959.1:c.1600T>G
ENST00000645553.1:c.1646T>G	ENSP00000494725.1:p.Leu549Ter
ENST00000646085.1:c.*1109T>G	ENSP00000494509.1:n.*1109T>G
ENST00000646277.1:c.*232T>G	ENSP00000495289.1:n.*232T>G
ENST00000646544.1:c.619T>G
ENST00000646699.1:c.1570T>G
ENST00000646793.1:c.1523T>G	ENSP00000494512.1:p.Leu508Ter
ENST00000361150.6:c.1634T>G	ENSP00000354781.2:p.Leu545Ter
ENST00000361510.6:c.1796T>G	ENSP00000355324.2:p.Leu599Ter
ENST00000361715.6:c.1688T>G	ENSP00000355311.2:p.Leu563Ter
ENST00000361828.6:c.1685T>G	ENSP00000354429.2:p.Leu562Ter
ENST00000361908.7:c.1742T>G	ENSP00000354681.3:p.Leu581Ter
ENST00000392438.7:c.1631T>G	ENSP00000376233.3:p.Leu544Ter
ENST00000483516.1:n.129T>G
NM_015560.2:c.1631T>G , LRG_337t1:c.1631T>G	NP_056375.2:p.Leu544Ter
NM_130831.2:c.1523T>G	NP_570844.1:p.Leu508Ter
NM_130832.2:c.1577T>G	NP_570845.1:p.Leu526Ter
NM_130833.2:c.1634T>G	NP_570846.1:p.Leu545Ter
NM_130834.2:c.1685T>G	NP_570847.2:p.Leu562Ter
NM_130835.2:c.1688T>G	NP_570848.1:p.Leu563Ter
NM_130836.2:c.1742T>G	NP_570849.2:p.Leu581Ter
NM_130837.2:c.1796T>G , LRG_337t2:c.1796T>G	NP_570850.2:p.Leu599Ter
XM_011512863.1:c.1796T>G	XP_011511165.1:p.Leu599Ter
XM_011512864.1:c.1742T>G	XP_011511166.1:p.Leu581Ter
XM_011512865.1:c.1685T>G	XP_011511167.1:p.Leu562Ter
XM_011512866.1:c.1634T>G	XP_011511168.1:p.Leu545Ter
XM_011512867.1:c.1631T>G	XP_011511169.1:p.Leu544Ter
XM_011512868.1:c.1523T>G	XP_011511170.1:p.Leu508Ter
XM_011512869.1:c.1796T>G	XP_011511171.1:p.Leu599Ter
NM_001354663.1:c.1262T>G	NP_001341592.1:p.Leu421Ter
NM_001354664.1:c.1259T>G	NP_001341593.1:p.Leu420Ter
XR_001740158.2:n.2025T>G
XR_001740159.2:n.1860T>G
NM_001354663.2:c.1262T>G	NP_001341592.1:p.Leu421Ter
NM_001354664.2:c.1259T>G	NP_001341593.1:p.Leu420Ter
NM_130831.3:c.1523T>G	NP_570844.1:p.Leu508Ter
NM_130832.3:c.1577T>G	NP_570845.1:p.Leu526Ter
NM_130834.3:c.1685T>G	NP_570847.2:p.Leu562Ter
NM_130836.3:c.1742T>G	NP_570849.2:p.Leu581Ter
NM_015560.3:c.1631T>G	NP_056375.2:p.Leu544Ter
NM_130833.3:c.1634T>G	NP_570846.1:p.Leu545Ter
NM_130835.3:c.1688T>G	NP_570848.1:p.Leu563Ter
NM_130837.3:c.1796T>G MANE Select	NP_570850.2:p.Leu599Ter