Canonical Allele Identifier: CA1633507926

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984391G= , CM000668.2:g.63984391G=	GRCh38
NC_000006.11:g.64694284G= , CM000668.1:g.64694284G=	GRCh37
NC_000006.10:g.64752243G=	NCBI36
NG_023443.1:g.1727835C=
NG_023443.2:g.1727835C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7047C= MANE Select	ENSP00000424243.1:p.Thr2349=
ENST00000370616.6:c.7047C=	ENSP00000359650.2:p.Thr2349=
ENST00000370618.7:c.7047C=	ENSP00000359652.4:p.Thr2349=
ENST00000370621.7:c.7047C=	ENSP00000359655.3:p.Thr2349=
ENST00000398580.3:c.361C=
ENST00000503581.5:c.7047C=	ENSP00000424243.1:p.Thr2349=
NM_001142800.1:c.7047C=	NP_001136272.1:p.Thr2349=
NM_001292009.1:c.7047C=	NP_001278938.1:p.Thr2349=
XR_001744188.1:n.606+16107G=
XR_001744189.1:n.129+16107G=
XR_001744190.1:n.197+16107G=
XR_001744191.1:n.607-1263G=
NM_001142800.2:c.7047C= MANE Select	NP_001136272.1:p.Thr2349=
NM_001292009.2:c.7047C=	NP_001278938.1:p.Thr2349=