Canonical Allele Identifier: CA140242861

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63778094G>A , CM000668.2:g.63778094G>A GRCh38
NC_000006.11:g.64487987G>A , CM000668.1:g.64487987G>A GRCh37
NC_000006.10:g.64545946G>A NCBI36
NG_023443.1:g.1934132C>T
NG_023443.2:g.1934132C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.7810C>T (EYS) MANE Select NP_001136272.1:p.Arg2604Cys
ENST00000503581.6:c.7810C>T (EYS) MANE Select ENSP00000424243.1:p.Arg2604Cys
NM_001142800.1:c.7810C>T (EYS) NP_001136272.1:p.Arg2604Cys
NM_001292009.1:c.7810C>T (EYS) NP_001278938.1:p.Arg2604Cys
NM_001292009.2:c.7810C>T (EYS) NP_001278938.1:p.Arg2604Cys
ENST00000370616.6:c.7810C>T (EYS) ENSP00000359650.2:p.Arg2604Cys
ENST00000370618.7:c.7810C>T (EYS) ENSP00000359652.4:p.Arg2604Cys
ENST00000370621.7:c.7810C>T (EYS) ENSP00000359655.3:p.Arg2604Cys
ENST00000398580.3:c.1124C>T (EYS)
ENST00000420043.1:n.490G>A (PHF3)
ENST00000503581.5:c.7810C>T (EYS) ENSP00000424243.1:p.Arg2604Cys
ENST00000505138.1:c.392G>A (PHF3)