Canonical Allele Identifier: CA2771459623
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63788247del , CM000668.2:g.63788247del GRCh38
NC_000006.11:g.64498140del , CM000668.1:g.64498140del GRCh37
NC_000006.10:g.64556099del NCBI36
NG_023443.1:g.1923979del
NG_023443.2:g.1923979del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.7581del MANE Select ENSP00000424243.1:p.Asp2528MetfsTer25
ENST00000370616.6:c.7581del ENSP00000359650.2:p.Asp2528MetfsTer25
ENST00000370618.7:c.7581del ENSP00000359652.4:p.Asp2528MetfsTer25
ENST00000370621.7:c.7581del ENSP00000359655.3:p.Asp2528MetfsTer25
ENST00000398580.3:c.895del
ENST00000486069.1:n.221del
ENST00000503581.5:c.7581del ENSP00000424243.1:p.Asp2528MetfsTer25
NM_001142800.1:c.7581del NP_001136272.1:p.Asp2528MetfsTer25
NM_001292009.1:c.7581del NP_001278938.1:p.Asp2528MetfsTer25
NM_001142800.2:c.7581del MANE Select NP_001136272.1:p.Asp2528MetfsTer25
NM_001292009.2:c.7581del NP_001278938.1:p.Asp2528MetfsTer25