Canonical Allele Identifier: CA2771464180

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984642_63984643insA , CM000668.2:g.63984642_63984643insA	GRCh38
NC_000006.11:g.64694535_64694536insA , CM000668.1:g.64694535_64694536insA	GRCh37
NC_000006.10:g.64752494_64752495insA	NCBI36
NG_023443.1:g.1727583_1727584insT
NG_023443.2:g.1727583_1727584insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-40_6835-39insT MANE Select	ENSP00000424243.1:n.6835-40_6835-39insT
ENST00000370616.6:c.6835-40_6835-39insT	ENSP00000359650.2:n.6835-40_6835-39insT
ENST00000370618.7:c.6835-40_6835-39insT	ENSP00000359652.4:n.6835-40_6835-39insT
ENST00000370621.7:c.6835-40_6835-39insT	ENSP00000359655.3:n.6835-40_6835-39insT
ENST00000398580.3:c.149-40_149-39insT
ENST00000503581.5:c.6835-40_6835-39insT	ENSP00000424243.1:n.6835-40_6835-39insT
NM_001142800.1:c.6835-40_6835-39insT	NP_001136272.1:n.6835-40_6835-39insT
NM_001292009.1:c.6835-40_6835-39insT	NP_001278938.1:n.6835-40_6835-39insT
XR_001744188.1:n.606+16358_606+16359insA
XR_001744189.1:n.129+16358_129+16359insA
XR_001744190.1:n.197+16358_197+16359insA
XR_001744191.1:n.607-1012_607-1011insA
NM_001142800.2:c.6835-40_6835-39insT MANE Select	NP_001136272.1:n.6835-40_6835-39insT
NM_001292009.2:c.6835-40_6835-39insT	NP_001278938.1:n.6835-40_6835-39insT