Canonical Allele Identifier: CA1633626628

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230601A= , CM000668.2:g.64230601A=	GRCh38
NC_000006.11:g.64940494A= , CM000668.1:g.64940494A=	GRCh37
NC_000006.10:g.64998453A=	NCBI36
NG_023443.1:g.1481625T=
NG_023443.2:g.1481625T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000503581.6:c.6415T= MANE Select	ENSP00000424243.1:p.Cys2139=
ENST00000370616.6:c.6415T=	ENSP00000359650.2:p.Cys2139=
ENST00000370618.7:c.6415T=	ENSP00000359652.4:p.Cys2139=
ENST00000370621.7:c.6415T=	ENSP00000359655.3:p.Cys2139=
ENST00000503581.5:c.6415T=	ENSP00000424243.1:p.Cys2139=
NM_001142800.1:c.6415T=	NP_001136272.1:p.Cys2139=
NM_001292009.1:c.6415T=	NP_001278938.1:p.Cys2139=
NM_001142800.2:c.6415T= MANE Select	NP_001136272.1:p.Cys2139=
NM_001292009.2:c.6415T=	NP_001278938.1:p.Cys2139=