Canonical Allele Identifier: CA364786663

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64813377C>T , CM000668.2:g.64813377C>T	GRCh38
NC_000006.11:g.65523270C>T , CM000668.1:g.65523270C>T	GRCh37
NC_000006.10:g.65579991C>T	NCBI36
NG_023443.1:g.898849G>A
NG_023443.2:g.898849G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001142800.2:c.3443+1G>A MANE Select	NP_001136272.1:n.3443+1G>A
ENST00000503581.6:c.3443+1G>A MANE Select	ENSP00000424243.1:n.3443+1G>A
NM_001142800.1:c.3443+1G>A	NP_001136272.1:n.3443+1G>A
NM_001292009.1:c.3443+1G>A	NP_001278938.1:n.3443+1G>A
NM_001292009.2:c.3443+1G>A	NP_001278938.1:n.3443+1G>A
ENST00000370616.6:c.3443+1G>A	ENSP00000359650.2:n.3443+1G>A
ENST00000370618.7:c.3443+1G>A	ENSP00000359652.4:n.3443+1G>A
ENST00000370621.7:c.3443+1G>A	ENSP00000359655.3:n.3443+1G>A
ENST00000503581.5:c.3443+1G>A	ENSP00000424243.1:n.3443+1G>A