Canonical Allele Identifier: CA2771459727

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788360_63788361insACAA , CM000668.2:g.63788360_63788361insACAA	GRCh38
NC_000006.11:g.64498253_64498254insACAA , CM000668.1:g.64498253_64498254insACAA	GRCh37
NC_000006.10:g.64556212_64556213insACAA	NCBI36
NG_023443.1:g.1923865_1923866insTTGT
NG_023443.2:g.1923865_1923866insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7579-112_7579-111insTTGT MANE Select	ENSP00000424243.1:n.7579-112_7579-111insTTGT
ENST00000370616.6:c.7579-112_7579-111insTTGT	ENSP00000359650.2:n.7579-112_7579-111insTTGT
ENST00000370618.7:c.7579-112_7579-111insTTGT	ENSP00000359652.4:n.7579-112_7579-111insTTGT
ENST00000370621.7:c.7579-112_7579-111insTTGT	ENSP00000359655.3:n.7579-112_7579-111insTTGT
ENST00000398580.3:c.893-112_893-111insTTGT
ENST00000486069.1:n.219-112_219-111insTTGT
ENST00000503581.5:c.7579-112_7579-111insTTGT	ENSP00000424243.1:n.7579-112_7579-111insTTGT
NM_001142800.1:c.7579-112_7579-111insTTGT	NP_001136272.1:n.7579-112_7579-111insTTGT
NM_001292009.1:c.7579-112_7579-111insTTGT	NP_001278938.1:n.7579-112_7579-111insTTGT
NM_001142800.2:c.7579-112_7579-111insTTGT MANE Select	NP_001136272.1:n.7579-112_7579-111insTTGT
NM_001292009.2:c.7579-112_7579-111insTTGT	NP_001278938.1:n.7579-112_7579-111insTTGT