Canonical Allele Identifier: CA2739273206

Gene: EYS

Linked Data

• ClinVar Variation Id: 2813754
• ClinVar RCV Id: RCV003680587

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788255A>T , CM000668.2:g.63788255A>T	GRCh38
NC_000006.11:g.64498148A>T , CM000668.1:g.64498148A>T	GRCh37
NC_000006.10:g.64556107A>T	NCBI36
NG_023443.1:g.1923971T>A
NG_023443.2:g.1923971T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7579-6T>A MANE Select	ENSP00000424243.1:n.7579-6T>A
ENST00000370616.6:c.7579-6T>A	ENSP00000359650.2:n.7579-6T>A
ENST00000370618.7:c.7579-6T>A	ENSP00000359652.4:n.7579-6T>A
ENST00000370621.7:c.7579-6T>A	ENSP00000359655.3:n.7579-6T>A
ENST00000398580.3:c.893-6T>A
ENST00000486069.1:n.219-6T>A
ENST00000503581.5:c.7579-6T>A	ENSP00000424243.1:n.7579-6T>A
NM_001142800.1:c.7579-6T>A	NP_001136272.1:n.7579-6T>A
NM_001292009.1:c.7579-6T>A	NP_001278938.1:n.7579-6T>A
NM_001142800.2:c.7579-6T>A MANE Select	NP_001136272.1:n.7579-6T>A
NM_001292009.2:c.7579-6T>A	NP_001278938.1:n.7579-6T>A