Canonical Allele Identifier: CA2771464262

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984710_63984711insACA , CM000668.2:g.63984710_63984711insACA	GRCh38
NC_000006.11:g.64694603_64694604insACA , CM000668.1:g.64694603_64694604insACA	GRCh37
NC_000006.10:g.64752562_64752563insACA	NCBI36
NG_023443.1:g.1727515_1727516insTGT
NG_023443.2:g.1727515_1727516insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-108_6835-107insTGT MANE Select	ENSP00000424243.1:n.6835-108_6835-107insTGT
ENST00000370616.6:c.6835-108_6835-107insTGT	ENSP00000359650.2:n.6835-108_6835-107insTGT
ENST00000370618.7:c.6835-108_6835-107insTGT	ENSP00000359652.4:n.6835-108_6835-107insTGT
ENST00000370621.7:c.6835-108_6835-107insTGT	ENSP00000359655.3:n.6835-108_6835-107insTGT
ENST00000398580.3:c.149-108_149-107insTGT
ENST00000503581.5:c.6835-108_6835-107insTGT	ENSP00000424243.1:n.6835-108_6835-107insTGT
NM_001142800.1:c.6835-108_6835-107insTGT	NP_001136272.1:n.6835-108_6835-107insTGT
NM_001292009.1:c.6835-108_6835-107insTGT	NP_001278938.1:n.6835-108_6835-107insTGT
XR_001744188.1:n.606+16426_606+16427insACA
XR_001744189.1:n.129+16426_129+16427insACA
XR_001744190.1:n.197+16426_197+16427insACA
XR_001744191.1:n.607-944_607-943insACA
NM_001142800.2:c.6835-108_6835-107insTGT MANE Select	NP_001136272.1:n.6835-108_6835-107insTGT
NM_001292009.2:c.6835-108_6835-107insTGT	NP_001278938.1:n.6835-108_6835-107insTGT