Canonical Allele Identifier: CA1633809424
Community Standard Title: NM_001142800.2(EYS):c.4387A= (p.Arg1463=)
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64591480T= , CM000668.2:g.64591480T= GRCh38
NC_000006.11:g.65301373T= , CM000668.1:g.65301373T= GRCh37
NC_000006.10:g.65358094T= NCBI36
NG_023443.1:g.1120746A=
NG_023443.2:g.1120746A=

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.4387A= MANE Select NP_001136272.1:p.Arg1463=
ENST00000503581.6:c.4387A= MANE Select ENSP00000424243.1:p.Arg1463=
NM_001142800.1:c.4387A= NP_001136272.1:p.Arg1463=
NM_001292009.1:c.4387A= NP_001278938.1:p.Arg1463=
NM_001292009.2:c.4387A= NP_001278938.1:p.Arg1463=
ENST00000370616.6:c.4387A= ENSP00000359650.2:p.Arg1463=
ENST00000370618.7:c.4387A= ENSP00000359652.4:p.Arg1463=
ENST00000370621.7:c.4387A= ENSP00000359655.3:p.Arg1463=
ENST00000503581.5:c.4387A= ENSP00000424243.1:p.Arg1463=