Canonical Allele Identifier: CA2771464258

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984707_63984708insACA , CM000668.2:g.63984707_63984708insACA	GRCh38
NC_000006.11:g.64694600_64694601insACA , CM000668.1:g.64694600_64694601insACA	GRCh37
NC_000006.10:g.64752559_64752560insACA	NCBI36
NG_023443.1:g.1727518_1727519insTGT
NG_023443.2:g.1727518_1727519insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-105_6835-104insTGT MANE Select	ENSP00000424243.1:n.6835-105_6835-104insTGT
ENST00000370616.6:c.6835-105_6835-104insTGT	ENSP00000359650.2:n.6835-105_6835-104insTGT
ENST00000370618.7:c.6835-105_6835-104insTGT	ENSP00000359652.4:n.6835-105_6835-104insTGT
ENST00000370621.7:c.6835-105_6835-104insTGT	ENSP00000359655.3:n.6835-105_6835-104insTGT
ENST00000398580.3:c.149-105_149-104insTGT
ENST00000503581.5:c.6835-105_6835-104insTGT	ENSP00000424243.1:n.6835-105_6835-104insTGT
NM_001142800.1:c.6835-105_6835-104insTGT	NP_001136272.1:n.6835-105_6835-104insTGT
NM_001292009.1:c.6835-105_6835-104insTGT	NP_001278938.1:n.6835-105_6835-104insTGT
XR_001744188.1:n.606+16423_606+16424insACA
XR_001744189.1:n.129+16423_129+16424insACA
XR_001744190.1:n.197+16423_197+16424insACA
XR_001744191.1:n.607-947_607-946insACA
NM_001142800.2:c.6835-105_6835-104insTGT MANE Select	NP_001136272.1:n.6835-105_6835-104insTGT
NM_001292009.2:c.6835-105_6835-104insTGT	NP_001278938.1:n.6835-105_6835-104insTGT