Canonical Allele Identifier: CA1633554871
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64081821C= , CM000668.2:g.64081821C= GRCh38
NC_000006.11:g.64791714C= , CM000668.1:g.64791714C= GRCh37
NC_000006.10:g.64849673C= NCBI36
NG_023443.1:g.1630405G=
NG_023443.2:g.1630405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6571+35G= MANE Select ENSP00000424243.1:n.6571+35G=
ENST00000370616.6:c.6571+35G= ENSP00000359650.2:n.6571+35G=
ENST00000370618.7:c.6571+35G= ENSP00000359652.4:n.6571+35G=
ENST00000370621.7:c.6571+35G= ENSP00000359655.3:n.6571+35G=
ENST00000503581.5:c.6571+35G= ENSP00000424243.1:n.6571+35G=
NM_001142800.1:c.6571+35G= NP_001136272.1:n.6571+35G=
NM_001292009.1:c.6571+35G= NP_001278938.1:n.6571+35G=
NM_001142800.2:c.6571+35G= MANE Select NP_001136272.1:n.6571+35G=
NM_001292009.2:c.6571+35G= NP_001278938.1:n.6571+35G=