Canonical Allele Identifier: CA355788153

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193355751T>A (hg19) ; chr3:g.193637962T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193637962T>A , CM000665.2:g.193637962T>A	GRCh38
NC_000003.11:g.193355751T>A , CM000665.1:g.193355751T>A	GRCh37
NC_000003.10:g.194838445T>A	NCBI36
NG_011605.1:g.49819T>A , LRG_337:g.49819T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1046T>A MANE Select	ENSP00000355324.2:p.Val349Asp
ENST00000361828.7:c.881T>A	ENSP00000354429.3:p.Val294Asp
ENST00000361908.8:c.992T>A	ENSP00000354681.3:p.Val331Asp
ENST00000392436.7:c.881T>A	ENSP00000376231.3:p.Val294Asp
ENST00000392437.6:c.935T>A	ENSP00000376232.2:p.Val312Asp
ENST00000642289.1:c.976T>A
ENST00000642445.1:c.881T>A	ENSP00000495535.1:p.Val294Asp
ENST00000642593.1:c.881T>A	ENSP00000494273.1:p.Val294Asp
ENST00000643329.1:c.563T>A	ENSP00000493673.1:p.Val188Asp
ENST00000643737.1:c.*962T>A	ENSP00000494210.1:n.*962T>A
ENST00000644595.1:c.881T>A	ENSP00000494121.1:p.Val294Asp
ENST00000644629.1:c.541T>A
ENST00000644841.1:c.509T>A	ENSP00000493988.1:p.Val170Asp
ENST00000644959.1:c.850T>A
ENST00000645553.1:c.896T>A	ENSP00000494725.1:p.Val299Asp
ENST00000646085.1:c.*359T>A	ENSP00000494509.1:n.*359T>A
ENST00000646277.1:c.1046T>A	ENSP00000495289.1:p.Val349Asp
ENST00000646699.1:c.976T>A
ENST00000646793.1:c.773T>A	ENSP00000494512.1:p.Val258Asp
ENST00000361150.6:c.884T>A	ENSP00000354781.2:p.Val295Asp
ENST00000361510.6:c.1046T>A	ENSP00000355324.2:p.Val349Asp
ENST00000361715.6:c.938T>A	ENSP00000355311.2:p.Val313Asp
ENST00000361828.6:c.935T>A	ENSP00000354429.2:p.Val312Asp
ENST00000361908.7:c.992T>A	ENSP00000354681.3:p.Val331Asp
ENST00000392438.7:c.881T>A	ENSP00000376233.3:p.Val294Asp
ENST00000475899.1:n.77T>A
ENST00000495476.1:n.402T>A
ENST00000497189.5:n.367T>A
NM_015560.2:c.881T>A , LRG_337t1:c.881T>A	NP_056375.2:p.Val294Asp
NM_130831.2:c.773T>A	NP_570844.1:p.Val258Asp
NM_130832.2:c.827T>A	NP_570845.1:p.Val276Asp
NM_130833.2:c.884T>A	NP_570846.1:p.Val295Asp
NM_130834.2:c.935T>A	NP_570847.2:p.Val312Asp
NM_130835.2:c.938T>A	NP_570848.1:p.Val313Asp
NM_130836.2:c.992T>A	NP_570849.2:p.Val331Asp
NM_130837.2:c.1046T>A , LRG_337t2:c.1046T>A	NP_570850.2:p.Val349Asp
XM_011512863.1:c.1046T>A	XP_011511165.1:p.Val349Asp
XM_011512864.1:c.992T>A	XP_011511166.1:p.Val331Asp
XM_011512865.1:c.935T>A	XP_011511167.1:p.Val312Asp
XM_011512866.1:c.884T>A	XP_011511168.1:p.Val295Asp
XM_011512867.1:c.881T>A	XP_011511169.1:p.Val294Asp
XM_011512868.1:c.773T>A	XP_011511170.1:p.Val258Asp
XM_011512869.1:c.1046T>A	XP_011511171.1:p.Val349Asp
NM_001354663.1:c.512T>A	NP_001341592.1:p.Val171Asp
NM_001354664.1:c.509T>A	NP_001341593.1:p.Val170Asp
XR_001740158.2:n.1275T>A
XR_001740159.2:n.1110T>A
NM_001354663.2:c.512T>A	NP_001341592.1:p.Val171Asp
NM_001354664.2:c.509T>A	NP_001341593.1:p.Val170Asp
NM_130831.3:c.773T>A	NP_570844.1:p.Val258Asp
NM_130832.3:c.827T>A	NP_570845.1:p.Val276Asp
NM_130834.3:c.935T>A	NP_570847.2:p.Val312Asp
NM_130836.3:c.992T>A	NP_570849.2:p.Val331Asp
NM_015560.3:c.881T>A	NP_056375.2:p.Val294Asp
NM_130833.3:c.884T>A	NP_570846.1:p.Val295Asp
NM_130835.3:c.938T>A	NP_570848.1:p.Val313Asp
NM_130837.3:c.1046T>A MANE Select	NP_570850.2:p.Val349Asp