Canonical Allele Identifier: CA2771469823
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230828_64230829insA , CM000668.2:g.64230828_64230829insA GRCh38
NC_000006.11:g.64940721_64940722insA , CM000668.1:g.64940721_64940722insA GRCh37
NC_000006.10:g.64998680_64998681insA NCBI36
NG_023443.1:g.1481397_1481398insT
NG_023443.2:g.1481397_1481398insT

Transcript Alleles

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