Canonical Allele Identifier: CA2771459723

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788350_63788351insAGG , CM000668.2:g.63788350_63788351insAGG	GRCh38
NC_000006.11:g.64498243_64498244insAGG , CM000668.1:g.64498243_64498244insAGG	GRCh37
NC_000006.10:g.64556202_64556203insAGG	NCBI36
NG_023443.1:g.1923875_1923876insCCT
NG_023443.2:g.1923875_1923876insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7579-102_7579-101insCCT MANE Select	ENSP00000424243.1:n.7579-102_7579-101insCCT
ENST00000370616.6:c.7579-102_7579-101insCCT	ENSP00000359650.2:n.7579-102_7579-101insCCT
ENST00000370618.7:c.7579-102_7579-101insCCT	ENSP00000359652.4:n.7579-102_7579-101insCCT
ENST00000370621.7:c.7579-102_7579-101insCCT	ENSP00000359655.3:n.7579-102_7579-101insCCT
ENST00000398580.3:c.893-102_893-101insCCT
ENST00000486069.1:n.219-102_219-101insCCT
ENST00000503581.5:c.7579-102_7579-101insCCT	ENSP00000424243.1:n.7579-102_7579-101insCCT
NM_001142800.1:c.7579-102_7579-101insCCT	NP_001136272.1:n.7579-102_7579-101insCCT
NM_001292009.1:c.7579-102_7579-101insCCT	NP_001278938.1:n.7579-102_7579-101insCCT
NM_001142800.2:c.7579-102_7579-101insCCT MANE Select	NP_001136272.1:n.7579-102_7579-101insCCT
NM_001292009.2:c.7579-102_7579-101insCCT	NP_001278938.1:n.7579-102_7579-101insCCT