Canonical Allele Identifier: CA2771464218

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984677_63984683del , CM000668.2:g.63984677_63984683del	GRCh38
NC_000006.11:g.64694570_64694576del , CM000668.1:g.64694570_64694576del	GRCh37
NC_000006.10:g.64752529_64752535del	NCBI36
NG_023443.1:g.1727543_1727549del
NG_023443.2:g.1727543_1727549del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6835-80_6835-74del MANE Select	ENSP00000424243.1:n.6835-80_6835-74del
ENST00000370616.6:c.6835-80_6835-74del	ENSP00000359650.2:n.6835-80_6835-74del
ENST00000370618.7:c.6835-80_6835-74del	ENSP00000359652.4:n.6835-80_6835-74del
ENST00000370621.7:c.6835-80_6835-74del	ENSP00000359655.3:n.6835-80_6835-74del
ENST00000398580.3:c.149-80_149-74del
ENST00000503581.5:c.6835-80_6835-74del	ENSP00000424243.1:n.6835-80_6835-74del
NM_001142800.1:c.6835-80_6835-74del	NP_001136272.1:n.6835-80_6835-74del
NM_001292009.1:c.6835-80_6835-74del	NP_001278938.1:n.6835-80_6835-74del
XR_001744188.1:n.606+16393_606+16399del
XR_001744189.1:n.129+16393_129+16399del
XR_001744190.1:n.197+16393_197+16399del
XR_001744191.1:n.607-977_607-971del
NM_001142800.2:c.6835-80_6835-74del MANE Select	NP_001136272.1:n.6835-80_6835-74del
NM_001292009.2:c.6835-80_6835-74del	NP_001278938.1:n.6835-80_6835-74del