Canonical Allele Identifier: CA364790483

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.65495237C>T , CM000668.2:g.65495237C>T	GRCh38
NC_000006.11:g.66205130C>T , CM000668.1:g.66205130C>T	GRCh37
NC_000006.10:g.66261851C>T	NCBI36
NG_023443.1:g.216989G>A
NG_023443.2:g.216989G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.174G>A MANE Select	ENSP00000424243.1:p.Trp58Ter
ENST00000342421.9:c.174G>A	ENSP00000341818.5:p.Trp58Ter
ENST00000370616.6:c.174G>A	ENSP00000359650.2:p.Trp58Ter
ENST00000370618.7:c.174G>A	ENSP00000359652.4:p.Trp58Ter
ENST00000370621.7:c.174G>A	ENSP00000359655.3:p.Trp58Ter
ENST00000393380.6:c.174G>A	ENSP00000377042.2:p.Trp58Ter
ENST00000471279.1:c.-136G>A	ENSP00000420530.1:n.-136G>A
ENST00000489873.1:n.701G>A
ENST00000503581.5:c.174G>A	ENSP00000424243.1:p.Trp58Ter
NM_001142800.1:c.174G>A	NP_001136272.1:p.Trp58Ter
NM_001142801.1:c.174G>A	NP_001136273.1:p.Trp58Ter
NM_001292009.1:c.174G>A	NP_001278938.1:p.Trp58Ter
NM_198283.1:c.174G>A	NP_938024.1:p.Trp58Ter
NM_001142800.2:c.174G>A MANE Select	NP_001136272.1:p.Trp58Ter
NM_001142801.2:c.174G>A	NP_001136273.1:p.Trp58Ter
NM_001292009.2:c.174G>A	NP_001278938.1:p.Trp58Ter
NM_198283.2:c.174G>A	NP_938024.1:p.Trp58Ter