Canonical Allele Identifier: CA12238376
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.65431130C>T , CM000668.2:g.65431130C>T GRCh38
NC_000006.11:g.66141023C>T , CM000668.1:g.66141023C>T GRCh37
NC_000006.10:g.66197744C>T NCBI36
NG_023443.1:g.281096G>A
NG_023443.2:g.281096G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.863-25763G>A MANE Select ENSP00000424243.1:n.863-25763G>A
ENST00000342421.9:c.863-25763G>A ENSP00000341818.5:n.863-25763G>A
ENST00000370616.6:c.863-25763G>A ENSP00000359650.2:n.863-25763G>A
ENST00000370618.7:c.863-25763G>A ENSP00000359652.4:n.863-25763G>A
ENST00000370621.7:c.863-25763G>A ENSP00000359655.3:n.863-25763G>A
ENST00000393380.6:c.863-25763G>A ENSP00000377042.2:n.863-25763G>A
ENST00000503581.5:c.863-25763G>A ENSP00000424243.1:n.863-25763G>A
NM_001142800.1:c.863-25763G>A NP_001136272.1:n.863-25763G>A
NM_001142801.1:c.863-25763G>A NP_001136273.1:n.863-25763G>A
NM_001292009.1:c.863-25763G>A NP_001278938.1:n.863-25763G>A
NM_198283.1:c.863-25763G>A NP_938024.1:n.863-25763G>A
NM_001142800.2:c.863-25763G>A MANE Select NP_001136272.1:n.863-25763G>A
NM_001142801.2:c.863-25763G>A NP_001136273.1:n.863-25763G>A
NM_001292009.2:c.863-25763G>A NP_001278938.1:n.863-25763G>A
NM_198283.2:c.863-25763G>A NP_938024.1:n.863-25763G>A