Canonical Allele Identifier: CA2771469867
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230881_64230882insGTC , CM000668.2:g.64230881_64230882insGTC GRCh38
NC_000006.11:g.64940774_64940775insGTC , CM000668.1:g.64940774_64940775insGTC GRCh37
NC_000006.10:g.64998733_64998734insGTC NCBI36
NG_023443.1:g.1481344_1481345insGAC
NG_023443.2:g.1481344_1481345insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6192-58_6192-57insGAC MANE Select ENSP00000424243.1:n.6192-58_6192-57insGAC
ENST00000370616.6:c.6192-58_6192-57insGAC ENSP00000359650.2:n.6192-58_6192-57insGAC
ENST00000370618.7:c.6192-58_6192-57insGAC ENSP00000359652.4:n.6192-58_6192-57insGAC
ENST00000370621.7:c.6192-58_6192-57insGAC ENSP00000359655.3:n.6192-58_6192-57insGAC
ENST00000503581.5:c.6192-58_6192-57insGAC ENSP00000424243.1:n.6192-58_6192-57insGAC
NM_001142800.1:c.6192-58_6192-57insGAC NP_001136272.1:n.6192-58_6192-57insGAC
NM_001292009.1:c.6192-58_6192-57insGAC NP_001278938.1:n.6192-58_6192-57insGAC
NM_001142800.2:c.6192-58_6192-57insGAC MANE Select NP_001136272.1:n.6192-58_6192-57insGAC
NM_001292009.2:c.6192-58_6192-57insGAC NP_001278938.1:n.6192-58_6192-57insGAC