Canonical Allele Identifier: CA364786377
Community Standard Title: NM_001142800.2(EYS):c.2499T>G (p.Phe833Leu)
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64912626A>C , CM000668.2:g.64912626A>C GRCh38
NC_000006.11:g.65622519A>C , CM000668.1:g.65622519A>C GRCh37
NC_000006.10:g.65679240A>C NCBI36
NG_023443.1:g.799600T>G
NG_023443.2:g.799600T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.2499T>G MANE Select NP_001136272.1:p.Phe833Leu
ENST00000503581.6:c.2499T>G MANE Select ENSP00000424243.1:p.Phe833Leu
NM_001142800.1:c.2499T>G NP_001136272.1:p.Phe833Leu
NM_001292009.1:c.2499T>G NP_001278938.1:p.Phe833Leu
NM_001292009.2:c.2499T>G NP_001278938.1:p.Phe833Leu
ENST00000370616.6:c.2499T>G ENSP00000359650.2:p.Phe833Leu
ENST00000370618.7:c.2499T>G ENSP00000359652.4:p.Phe833Leu
ENST00000370621.7:c.2499T>G ENSP00000359655.3:p.Phe833Leu
ENST00000503581.5:c.2499T>G ENSP00000424243.1:p.Phe833Leu