Canonical Allele Identifier: CA3876722
Community Standard Title: NM_001142800.2(EYS):c.8207C>T (p.Ala2736Val)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63726545G>A , CM000668.2:g.63726545G>A GRCh38
NC_000006.11:g.64436438G>A , CM000668.1:g.64436438G>A GRCh37
NC_000006.10:g.64494397G>A NCBI36
NG_023443.1:g.1985681C>T
NG_023443.2:g.1985681C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.8207C>T (EYS) MANE Select NP_001136272.1:p.Ala2736Val
ENST00000503581.6:c.8207C>T (EYS) MANE Select ENSP00000424243.1:p.Ala2736Val
NM_001142800.1:c.8207C>T (EYS) NP_001136272.1:p.Ala2736Val
NM_001292009.1:c.8270C>T (EYS) NP_001278938.1:p.Ala2757Val
NM_001292009.2:c.8270C>T (EYS) NP_001278938.1:p.Ala2757Val
ENST00000370616.6:c.8270C>T (EYS) ENSP00000359650.2:p.Ala2757Val
ENST00000370618.7:c.8207C>T (EYS) ENSP00000359652.4:p.Ala2736Val
ENST00000370621.7:c.8270C>T (EYS) ENSP00000359655.3:p.Ala2757Val
ENST00000503581.5:c.8207C>T (EYS) ENSP00000424243.1:p.Ala2736Val
ENST00000505138.1:c.363+15183G>A (PHF3)