Canonical Allele Identifier: CA548822895

Gene: OPA1

Linked Data

• dbSNP Id: rs1434249691
• gnomAD v2: 3-193364833-CT-C
• gnomAD v3: 3-193647044-CT-C
• gnomAD v4: 3-193647044-CT-C
• MyVariant Identifiers: chr3:g.193364834del (hg19) ; chr3:g.193647045del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193647046del , CM000665.2:g.193647046del	GRCh38
NC_000003.11:g.193364835del , CM000665.1:g.193364835del	GRCh37
NC_000003.10:g.194847529del	NCBI36
NG_011605.1:g.58903del , LRG_337:g.58903del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1755-19del MANE Select	ENSP00000355324.2:n.1755-19del
ENST00000361828.7:c.1590-19del	ENSP00000354429.3:n.1590-19del
ENST00000361908.8:c.1701-19del	ENSP00000354681.3:n.1701-19del
ENST00000392436.7:c.1590-19del	ENSP00000376231.3:n.1590-19del
ENST00000392437.6:c.1644-19del	ENSP00000376232.2:n.1644-19del
ENST00000642289.1:c.1529-19del
ENST00000642445.1:c.1590-19del	ENSP00000495535.1:n.1590-19del
ENST00000642593.1:c.1590-19del	ENSP00000494273.1:n.1590-19del
ENST00000643329.1:c.1272-19del	ENSP00000493673.1:n.1272-19del
ENST00000643737.1:c.*1671-19del	ENSP00000494210.1:n.*1671-19del
ENST00000644595.1:c.1590-19del	ENSP00000494121.1:n.1590-19del
ENST00000644629.1:c.1177-19del
ENST00000644841.1:c.*74-19del	ENSP00000493988.1:n.*74-19del
ENST00000644959.1:c.1559-19del
ENST00000645553.1:c.1605-19del	ENSP00000494725.1:n.1605-19del
ENST00000646085.1:c.*1068-19del	ENSP00000494509.1:n.*1068-19del
ENST00000646277.1:c.*191-19del	ENSP00000495289.1:n.*191-19del
ENST00000646544.1:c.578-19del
ENST00000646699.1:c.1529-19del
ENST00000646793.1:c.1482-19del	ENSP00000494512.1:n.1482-19del
ENST00000361150.6:c.1593-19del	ENSP00000354781.2:n.1593-19del
ENST00000361510.6:c.1755-19del	ENSP00000355324.2:n.1755-19del
ENST00000361715.6:c.1647-19del	ENSP00000355311.2:n.1647-19del
ENST00000361828.6:c.1644-19del	ENSP00000354429.2:n.1644-19del
ENST00000361908.7:c.1701-19del	ENSP00000354681.3:n.1701-19del
ENST00000392438.7:c.1590-19del	ENSP00000376233.3:n.1590-19del
ENST00000483516.1:n.88-19del
NM_015560.2:c.1590-19del , LRG_337t1:c.1590-19del	NP_056375.2:n.1590-19del
NM_130831.2:c.1482-19del	NP_570844.1:n.1482-19del
NM_130832.2:c.1536-19del	NP_570845.1:n.1536-19del
NM_130833.2:c.1593-19del	NP_570846.1:n.1593-19del
NM_130834.2:c.1644-19del	NP_570847.2:n.1644-19del
NM_130835.2:c.1647-19del	NP_570848.1:n.1647-19del
NM_130836.2:c.1701-19del	NP_570849.2:n.1701-19del
NM_130837.2:c.1755-19del , LRG_337t2:c.1755-19del	NP_570850.2:n.1755-19del
XM_011512863.1:c.1755-19del	XP_011511165.1:n.1755-19del
XM_011512864.1:c.1701-19del	XP_011511166.1:n.1701-19del
XM_011512865.1:c.1644-19del	XP_011511167.1:n.1644-19del
XM_011512866.1:c.1593-19del	XP_011511168.1:n.1593-19del
XM_011512867.1:c.1590-19del	XP_011511169.1:n.1590-19del
XM_011512868.1:c.1482-19del	XP_011511170.1:n.1482-19del
XM_011512869.1:c.1755-19del	XP_011511171.1:n.1755-19del
NM_001354663.1:c.1221-19del	NP_001341592.1:n.1221-19del
NM_001354664.1:c.1218-19del	NP_001341593.1:n.1218-19del
XR_001740158.2:n.1984-19del
XR_001740159.2:n.1819-19del
NM_001354663.2:c.1221-19del	NP_001341592.1:n.1221-19del
NM_001354664.2:c.1218-19del	NP_001341593.1:n.1218-19del
NM_130831.3:c.1482-19del	NP_570844.1:n.1482-19del
NM_130832.3:c.1536-19del	NP_570845.1:n.1536-19del
NM_130834.3:c.1644-19del	NP_570847.2:n.1644-19del
NM_130836.3:c.1701-19del	NP_570849.2:n.1701-19del
NM_015560.3:c.1590-19del	NP_056375.2:n.1590-19del
NM_130833.3:c.1593-19del	NP_570846.1:n.1593-19del
NM_130835.3:c.1647-19del	NP_570848.1:n.1647-19del
NM_130837.3:c.1755-19del MANE Select	NP_570850.2:n.1755-19del