Canonical Allele Identifier: CA364386174
Community Standard Title: NM_001142800.2(EYS):c.8143C>T (p.Arg2715Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63726609G>A , CM000668.2:g.63726609G>A GRCh38
NC_000006.11:g.64436502G>A , CM000668.1:g.64436502G>A GRCh37
NC_000006.10:g.64494461G>A NCBI36
NG_023443.1:g.1985617C>T
NG_023443.2:g.1985617C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.8143C>T (EYS) MANE Select NP_001136272.1:p.Arg2715Ter
ENST00000503581.6:c.8143C>T (EYS) MANE Select ENSP00000424243.1:p.Arg2715Ter
NM_001142800.1:c.8143C>T (EYS) NP_001136272.1:p.Arg2715Ter
NM_001292009.1:c.8206C>T (EYS) NP_001278938.1:p.Arg2736Ter
NM_001292009.2:c.8206C>T (EYS) NP_001278938.1:p.Arg2736Ter
ENST00000370616.6:c.8206C>T (EYS) ENSP00000359650.2:p.Arg2736Ter
ENST00000370618.7:c.8143C>T (EYS) ENSP00000359652.4:p.Arg2715Ter
ENST00000370621.7:c.8206C>T (EYS) ENSP00000359655.3:p.Arg2736Ter
ENST00000503581.5:c.8143C>T (EYS) ENSP00000424243.1:p.Arg2715Ter
ENST00000505138.1:c.363+15247G>A (PHF3)