Canonical Allele Identifier: CA364390376
Community Standard Title: NM_001142800.2(EYS):c.7899C>A (p.Tyr2633Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63762633G>T , CM000668.2:g.63762633G>T GRCh38
NC_000006.11:g.64472526G>T , CM000668.1:g.64472526G>T GRCh37
NC_000006.10:g.64530485G>T NCBI36
NG_023443.1:g.1949593C>A
NG_023443.2:g.1949593C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.7899C>A (EYS) MANE Select NP_001136272.1:p.Tyr2633Ter
ENST00000503581.6:c.7899C>A (EYS) MANE Select ENSP00000424243.1:p.Tyr2633Ter
NM_001142800.1:c.7899C>A (EYS) NP_001136272.1:p.Tyr2633Ter
NM_001292009.1:c.7899C>A (EYS) NP_001278938.1:p.Tyr2633Ter
NM_001292009.2:c.7899C>A (EYS) NP_001278938.1:p.Tyr2633Ter
ENST00000370616.6:c.7899C>A (EYS) ENSP00000359650.2:p.Tyr2633Ter
ENST00000370618.7:c.7899C>A (EYS) ENSP00000359652.4:p.Tyr2633Ter
ENST00000370621.7:c.7899C>A (EYS) ENSP00000359655.3:p.Tyr2633Ter
ENST00000398580.3:c.1213C>A (EYS)
ENST00000503581.5:c.7899C>A (EYS) ENSP00000424243.1:p.Tyr2633Ter
ENST00000505138.1:c.364-15433G>T (PHF3)