Canonical Allele Identifier: CA1633626687

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230745T= , CM000668.2:g.64230745T=	GRCh38
NC_000006.11:g.64940638T= , CM000668.1:g.64940638T=	GRCh37
NC_000006.10:g.64998597T=	NCBI36
NG_023443.1:g.1481481A=
NG_023443.2:g.1481481A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6271A= MANE Select	ENSP00000424243.1:p.Thr2091=
ENST00000370616.6:c.6271A=	ENSP00000359650.2:p.Thr2091=
ENST00000370618.7:c.6271A=	ENSP00000359652.4:p.Thr2091=
ENST00000370621.7:c.6271A=	ENSP00000359655.3:p.Thr2091=
ENST00000503581.5:c.6271A=	ENSP00000424243.1:p.Thr2091=
NM_001142800.1:c.6271A=	NP_001136272.1:p.Thr2091=
NM_001292009.1:c.6271A=	NP_001278938.1:p.Thr2091=
NM_001142800.2:c.6271A= MANE Select	NP_001136272.1:p.Thr2091=
NM_001292009.2:c.6271A=	NP_001278938.1:p.Thr2091=