Canonical Allele Identifier: CA377445615

Gene: OPN4

Linked Data

• dbSNP Id: rs1079610
• gnomAD v4: 10-86662359-C-A
• MyVariant Identifiers: chr10:g.88422116C>A (hg19) ; chr10:g.86662359C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86662359C>A , CM000672.2:g.86662359C>A	GRCh38
NC_000010.10:g.88422116C>A , CM000672.1:g.88422116C>A	GRCh37
NC_000010.9:g.88412096C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000372071.7:c.1214C>A	ENSP00000361141.2:p.Thr405Asn
ENST00000443292.2:c.1214C>A	ENSP00000393132.2:p.Thr405Asn
ENST00000685347.1:n.1176C>A
ENST00000690949.1:n.1215C>A
ENST00000241891.10:c.1181C>A MANE Select	ENSP00000241891.5:p.Thr394Asn
ENST00000241891.9:c.1181C>A	ENSP00000241891.5:p.Thr394Asn
ENST00000372071.6:c.1214C>A	ENSP00000361141.2:p.Thr405Asn
ENST00000443292.1:c.1214C>A	ENSP00000393132.1:p.Thr405Asn
NM_001030015.2:c.1214C>A	NP_001025186.1:p.Thr405Asn
NM_033282.3:c.1181C>A	NP_150598.1:p.Thr394Asn
XR_946165.1:n.150+559G>T
XM_017016955.1:c.1214C>A	XP_016872444.1:p.Thr405Asn
XM_017016956.1:c.1181C>A	XP_016872445.1:p.Thr394Asn
XM_017016957.1:c.962C>A	XP_016872446.1:p.Thr321Asn
XR_001747526.1:n.150+559G>T
NM_033282.4:c.1181C>A MANE Select	NP_150598.1:p.Thr394Asn
NM_001030015.3:c.1214C>A	NP_001025186.1:p.Thr405Asn