Canonical Allele Identifier: CA364789213

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.65490709T>C , CM000668.2:g.65490709T>C	GRCh38
NC_000006.11:g.66200602T>C , CM000668.1:g.66200602T>C	GRCh37
NC_000006.10:g.66257323T>C	NCBI36
NG_023443.1:g.221517A>G
NG_023443.2:g.221517A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001142800.2:c.749-2A>G MANE Select	NP_001136272.1:n.749-2A>G
ENST00000503581.6:c.749-2A>G MANE Select	ENSP00000424243.1:n.749-2A>G
NM_001142800.1:c.749-2A>G	NP_001136272.1:n.749-2A>G
NM_001142801.1:c.749-2A>G	NP_001136273.1:n.749-2A>G
NM_001142801.2:c.749-2A>G	NP_001136273.1:n.749-2A>G
NM_001292009.1:c.749-2A>G	NP_001278938.1:n.749-2A>G
NM_001292009.2:c.749-2A>G	NP_001278938.1:n.749-2A>G
NM_198283.1:c.749-2A>G	NP_938024.1:n.749-2A>G
NM_198283.2:c.749-2A>G	NP_938024.1:n.749-2A>G
ENST00000342421.9:c.749-2A>G	ENSP00000341818.5:n.749-2A>G
ENST00000370616.6:c.749-2A>G	ENSP00000359650.2:n.749-2A>G
ENST00000370618.7:c.749-2A>G	ENSP00000359652.4:n.749-2A>G
ENST00000370621.7:c.749-2A>G	ENSP00000359655.3:n.749-2A>G
ENST00000393380.6:c.749-2A>G	ENSP00000377042.2:n.749-2A>G
ENST00000471279.1:c.*214-2A>G	ENSP00000420530.1:n.*214-2A>G
ENST00000489873.1:n.1276-2A>G
ENST00000503581.5:c.749-2A>G	ENSP00000424243.1:n.749-2A>G