Canonical Allele Identifier: CA1633508062

Gene: EYS

Linked Data

• dbSNP Id: rs1582080454
• gnomAD v4: 6-63984676-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984676G>T , CM000668.2:g.63984676G>T	GRCh38
NC_000006.11:g.64694569G>T , CM000668.1:g.64694569G>T	GRCh37
NC_000006.10:g.64752528G>T	NCBI36
NG_023443.1:g.1727550C>A
NG_023443.2:g.1727550C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-73C>A MANE Select	ENSP00000424243.1:n.6835-73C>A
ENST00000370616.6:c.6835-73C>A	ENSP00000359650.2:n.6835-73C>A
ENST00000370618.7:c.6835-73C>A	ENSP00000359652.4:n.6835-73C>A
ENST00000370621.7:c.6835-73C>A	ENSP00000359655.3:n.6835-73C>A
ENST00000398580.3:c.149-73C>A
ENST00000503581.5:c.6835-73C>A	ENSP00000424243.1:n.6835-73C>A
NM_001142800.1:c.6835-73C>A	NP_001136272.1:n.6835-73C>A
NM_001292009.1:c.6835-73C>A	NP_001278938.1:n.6835-73C>A
XR_001744188.1:n.606+16392G>T
XR_001744189.1:n.129+16392G>T
XR_001744190.1:n.197+16392G>T
XR_001744191.1:n.607-978G>T
NM_001142800.2:c.6835-73C>A MANE Select	NP_001136272.1:n.6835-73C>A
NM_001292009.2:c.6835-73C>A	NP_001278938.1:n.6835-73C>A