Canonical Allele Identifier: CA468240668

Gene: OPTN

Linked Data

• MyVariant Identifiers: chr10:g.13168000T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13126000T>C , CM000672.2:g.13126000T>C	GRCh38
NC_000010.10:g.13168000T>C , CM000672.1:g.13168000T>C	GRCh37
NC_000010.9:g.13208006T>C	NCBI36
NG_012876.1:g.30919T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378747.8:c.1203T>C MANE Select	ENSP00000368021.3:p.Asn401=
ENST00000263036.9:c.1203T>C	ENSP00000263036.3:p.Asn401=
ENST00000378747.7:c.1203T>C	ENSP00000368021.3:p.Asn401=
ENST00000378748.7:c.1203T>C	ENSP00000368022.3:p.Asn401=
ENST00000378752.7:c.1185T>C	ENSP00000368027.3:p.Asn395=
ENST00000378757.6:c.1203T>C	ENSP00000368032.2:p.Asn401=
ENST00000378764.6:c.1185T>C	ENSP00000368040.1:p.Asn395=
NM_001008211.1:c.1203T>C	NP_001008212.1:p.Asn401=
NM_001008212.1:c.1203T>C	NP_001008213.1:p.Asn401=
NM_001008213.1:c.1203T>C	NP_001008214.1:p.Asn401=
NM_021980.4:c.1203T>C	NP_068815.2:p.Asn401=
XM_005252336.2:c.1185T>C	XP_005252393.2:p.Asn395=
XM_005252337.3:c.1185T>C	XP_005252394.2:p.Asn395=
XM_005252338.2:c.1032T>C	XP_005252395.2:p.Asn344=
NM_001008212.2:c.1203T>C MANE Select	NP_001008213.1:p.Asn401=