Canonical Allele Identifier: CA140244030
Community Standard Title: NM_001142800.2(EYS):c.7572G>A (p.Trp2524Ter)
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63789064C>T , CM000668.2:g.63789064C>T GRCh38
NC_000006.11:g.64498957C>T , CM000668.1:g.64498957C>T GRCh37
NC_000006.10:g.64556916C>T NCBI36
NG_023443.1:g.1923162G>A
NG_023443.2:g.1923162G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.7572G>A MANE Select NP_001136272.1:p.Trp2524Ter
ENST00000503581.6:c.7572G>A MANE Select ENSP00000424243.1:p.Trp2524Ter
NM_001142800.1:c.7572G>A NP_001136272.1:p.Trp2524Ter
NM_001292009.1:c.7572G>A NP_001278938.1:p.Trp2524Ter
NM_001292009.2:c.7572G>A NP_001278938.1:p.Trp2524Ter
ENST00000370616.6:c.7572G>A ENSP00000359650.2:p.Trp2524Ter
ENST00000370618.7:c.7572G>A ENSP00000359652.4:p.Trp2524Ter
ENST00000370621.7:c.7572G>A ENSP00000359655.3:p.Trp2524Ter
ENST00000398580.3:c.886G>A
ENST00000486069.1:n.212G>A
ENST00000503581.5:c.7572G>A ENSP00000424243.1:p.Trp2524Ter