Canonical Allele Identifier: CA140266929

Gene: EYS

Linked Data

• ClinVar Variation Id: 1265759
• ClinVar RCV Id: RCV001675055
• dbSNP Id: rs1482457
• gnomAD v2: 6-64694560-G-A
• gnomAD v3: 6-63984667-G-A
• gnomAD v4: 6-63984667-G-A
• MyVariant Identifiers: chr6:g.64694560G>A (hg19) ; chr6:g.63984667G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984667G>A , CM000668.2:g.63984667G>A	GRCh38
NC_000006.11:g.64694560G>A , CM000668.1:g.64694560G>A	GRCh37
NC_000006.10:g.64752519G>A	NCBI36
NG_023443.1:g.1727559C>T
NG_023443.2:g.1727559C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-64C>T MANE Select	ENSP00000424243.1:n.6835-64C>T
ENST00000370616.6:c.6835-64C>T	ENSP00000359650.2:n.6835-64C>T
ENST00000370618.7:c.6835-64C>T	ENSP00000359652.4:n.6835-64C>T
ENST00000370621.7:c.6835-64C>T	ENSP00000359655.3:n.6835-64C>T
ENST00000398580.3:c.149-64C>T
ENST00000503581.5:c.6835-64C>T	ENSP00000424243.1:n.6835-64C>T
NM_001142800.1:c.6835-64C>T	NP_001136272.1:n.6835-64C>T
NM_001292009.1:c.6835-64C>T	NP_001278938.1:n.6835-64C>T
XR_001744188.1:n.606+16383G>A
XR_001744189.1:n.129+16383G>A
XR_001744190.1:n.197+16383G>A
XR_001744191.1:n.607-987G>A
NM_001142800.2:c.6835-64C>T MANE Select	NP_001136272.1:n.6835-64C>T
NM_001292009.2:c.6835-64C>T	NP_001278938.1:n.6835-64C>T