Canonical Allele Identifier: CA2771469825
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230833_64230837del , CM000668.2:g.64230833_64230837del GRCh38
NC_000006.11:g.64940726_64940730del , CM000668.1:g.64940726_64940730del GRCh37
NC_000006.10:g.64998685_64998689del NCBI36
NG_023443.1:g.1481389_1481393del
NG_023443.2:g.1481389_1481393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6192-13_6192-9del MANE Select ENSP00000424243.1:n.6192-13_6192-9del
ENST00000370616.6:c.6192-13_6192-9del ENSP00000359650.2:n.6192-13_6192-9del
ENST00000370618.7:c.6192-13_6192-9del ENSP00000359652.4:n.6192-13_6192-9del
ENST00000370621.7:c.6192-13_6192-9del ENSP00000359655.3:n.6192-13_6192-9del
ENST00000503581.5:c.6192-13_6192-9del ENSP00000424243.1:n.6192-13_6192-9del
NM_001142800.1:c.6192-13_6192-9del NP_001136272.1:n.6192-13_6192-9del
NM_001292009.1:c.6192-13_6192-9del NP_001278938.1:n.6192-13_6192-9del
NM_001142800.2:c.6192-13_6192-9del MANE Select NP_001136272.1:n.6192-13_6192-9del
NM_001292009.2:c.6192-13_6192-9del NP_001278938.1:n.6192-13_6192-9del