Canonical Allele Identifier: CA3877145
Community Standard Title: NM_001142800.2(EYS):c.3586T>C (p.Cys1196Arg)
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64617516A>G , CM000668.2:g.64617516A>G GRCh38
NC_000006.11:g.65327409A>G , CM000668.1:g.65327409A>G GRCh37
NC_000006.10:g.65384130A>G NCBI36
NG_023443.1:g.1094710T>C
NG_023443.2:g.1094710T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.3586T>C MANE Select NP_001136272.1:p.Cys1196Arg
ENST00000503581.6:c.3586T>C MANE Select ENSP00000424243.1:p.Cys1196Arg
NM_001142800.1:c.3586T>C NP_001136272.1:p.Cys1196Arg
NM_001292009.1:c.3586T>C NP_001278938.1:p.Cys1196Arg
NM_001292009.2:c.3586T>C NP_001278938.1:p.Cys1196Arg
ENST00000330816.5:n.207T>C
ENST00000370616.6:c.3586T>C ENSP00000359650.2:p.Cys1196Arg
ENST00000370618.7:c.3586T>C ENSP00000359652.4:p.Cys1196Arg
ENST00000370621.7:c.3586T>C ENSP00000359655.3:p.Cys1196Arg
ENST00000503581.5:c.3586T>C ENSP00000424243.1:p.Cys1196Arg