Canonical Allele Identifier: CA2679283470
Gene: EYS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230787del , CM000668.2:g.64230787del GRCh38
NC_000006.11:g.64940680del , CM000668.1:g.64940680del GRCh37
NC_000006.10:g.64998639del NCBI36
NG_023443.1:g.1481439del
NG_023443.2:g.1481439del

Transcript Alleles

HGVS Amino-acid change
ENST00000503581.6:c.6229del MANE Select ENSP00000424243.1:p.Val2077LeufsTer6
ENST00000370616.6:c.6229del ENSP00000359650.2:p.Val2077LeufsTer6
ENST00000370618.7:c.6229del ENSP00000359652.4:p.Val2077LeufsTer6
ENST00000370621.7:c.6229del ENSP00000359655.3:p.Val2077LeufsTer6
ENST00000503581.5:c.6229del ENSP00000424243.1:p.Val2077LeufsTer6
NM_001142800.1:c.6229del NP_001136272.1:p.Val2077LeufsTer6
NM_001292009.1:c.6229del NP_001278938.1:p.Val2077LeufsTer6
NM_001142800.2:c.6229del MANE Select NP_001136272.1:p.Val2077LeufsTer6
NM_001292009.2:c.6229del NP_001278938.1:p.Val2077LeufsTer6