Canonical Allele Identifier: CA913111500
Gene: EYS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230777_64230787del , CM000668.2:g.64230777_64230787del GRCh38
NC_000006.11:g.64940670_64940680del , CM000668.1:g.64940670_64940680del GRCh37
NC_000006.10:g.64998629_64998639del NCBI36
NG_023443.1:g.1481439_1481449del
NG_023443.2:g.1481439_1481449del

Transcript Alleles

HGVS Amino-acid change
ENST00000503581.6:c.6229_6239del MANE Select ENSP00000424243.1:p.Val2077Ter
ENST00000370616.6:c.6229_6239del ENSP00000359650.2:p.Val2077Ter
ENST00000370618.7:c.6229_6239del ENSP00000359652.4:p.Val2077Ter
ENST00000370621.7:c.6229_6239del ENSP00000359655.3:p.Val2077Ter
ENST00000503581.5:c.6229_6239del ENSP00000424243.1:p.Val2077Ter
NM_001142800.1:c.6229_6239del NP_001136272.1:p.Val2077Ter
NM_001292009.1:c.6229_6239del NP_001278938.1:p.Val2077Ter
NM_001142800.2:c.6229_6239del MANE Select NP_001136272.1:p.Val2077Ter
NM_001292009.2:c.6229_6239del NP_001278938.1:p.Val2077Ter