Canonical Allele Identifier: CA2578660007
Gene: EYS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64081822A>T , CM000668.2:g.64081822A>T GRCh38
NC_000006.11:g.64791715A>T , CM000668.1:g.64791715A>T GRCh37
NC_000006.10:g.64849674A>T NCBI36
NG_023443.1:g.1630404T>A
NG_023443.2:g.1630404T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6571+34T>A MANE Select ENSP00000424243.1:n.6571+34T>A
ENST00000370616.6:c.6571+34T>A ENSP00000359650.2:n.6571+34T>A
ENST00000370618.7:c.6571+34T>A ENSP00000359652.4:n.6571+34T>A
ENST00000370621.7:c.6571+34T>A ENSP00000359655.3:n.6571+34T>A
ENST00000503581.5:c.6571+34T>A ENSP00000424243.1:n.6571+34T>A
NM_001142800.1:c.6571+34T>A NP_001136272.1:n.6571+34T>A
NM_001292009.1:c.6571+34T>A NP_001278938.1:n.6571+34T>A
NM_001142800.2:c.6571+34T>A MANE Select NP_001136272.1:n.6571+34T>A
NM_001292009.2:c.6571+34T>A NP_001278938.1:n.6571+34T>A
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