Canonical Allele Identifier: CA2679283513
Gene: EYS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230909_64230913del , CM000668.2:g.64230909_64230913del GRCh38
NC_000006.11:g.64940802_64940806del , CM000668.1:g.64940802_64940806del GRCh37
NC_000006.10:g.64998761_64998765del NCBI36
NG_023443.1:g.1481316_1481320del
NG_023443.2:g.1481316_1481320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6192-86_6192-82del MANE Select ENSP00000424243.1:n.6192-86_6192-82del
ENST00000370616.6:c.6192-86_6192-82del ENSP00000359650.2:n.6192-86_6192-82del
ENST00000370618.7:c.6192-86_6192-82del ENSP00000359652.4:n.6192-86_6192-82del
ENST00000370621.7:c.6192-86_6192-82del ENSP00000359655.3:n.6192-86_6192-82del
ENST00000503581.5:c.6192-86_6192-82del ENSP00000424243.1:n.6192-86_6192-82del
NM_001142800.1:c.6192-86_6192-82del NP_001136272.1:n.6192-86_6192-82del
NM_001292009.1:c.6192-86_6192-82del NP_001278938.1:n.6192-86_6192-82del
NM_001142800.2:c.6192-86_6192-82del MANE Select NP_001136272.1:n.6192-86_6192-82del
NM_001292009.2:c.6192-86_6192-82del NP_001278938.1:n.6192-86_6192-82del