Canonical Allele Identifier: CA1633626662
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230694A= , CM000668.2:g.64230694A= GRCh38
NC_000006.11:g.64940587A= , CM000668.1:g.64940587A= GRCh37
NC_000006.10:g.64998546A= NCBI36
NG_023443.1:g.1481532T=
NG_023443.2:g.1481532T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6322T= MANE Select ENSP00000424243.1:p.Cys2108=
ENST00000370616.6:c.6322T= ENSP00000359650.2:p.Cys2108=
ENST00000370618.7:c.6322T= ENSP00000359652.4:p.Cys2108=
ENST00000370621.7:c.6322T= ENSP00000359655.3:p.Cys2108=
ENST00000503581.5:c.6322T= ENSP00000424243.1:p.Cys2108=
NM_001142800.1:c.6322T= NP_001136272.1:p.Cys2108=
NM_001292009.1:c.6322T= NP_001278938.1:p.Cys2108=
NM_001142800.2:c.6322T= MANE Select NP_001136272.1:p.Cys2108=
NM_001292009.2:c.6322T= NP_001278938.1:p.Cys2108=