Canonical Allele Identifier: CA364391539
Gene: EYS HGNC NCBI

Linked Data

gnomAD v4: 6-64230775-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230775C>A , CM000668.2:g.64230775C>A GRCh38
NC_000006.11:g.64940668C>A , CM000668.1:g.64940668C>A GRCh37
NC_000006.10:g.64998627C>A NCBI36
NG_023443.1:g.1481451G>T
NG_023443.2:g.1481451G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6241G>T MANE Select ENSP00000424243.1:p.Asp2081Tyr
ENST00000370616.6:c.6241G>T ENSP00000359650.2:p.Asp2081Tyr
ENST00000370618.7:c.6241G>T ENSP00000359652.4:p.Asp2081Tyr
ENST00000370621.7:c.6241G>T ENSP00000359655.3:p.Asp2081Tyr
ENST00000503581.5:c.6241G>T ENSP00000424243.1:p.Asp2081Tyr
NM_001142800.1:c.6241G>T NP_001136272.1:p.Asp2081Tyr
NM_001292009.1:c.6241G>T NP_001278938.1:p.Asp2081Tyr
NM_001142800.2:c.6241G>T MANE Select NP_001136272.1:p.Asp2081Tyr
NM_001292009.2:c.6241G>T NP_001278938.1:p.Asp2081Tyr