Canonical Allele Identifier: CA1633508082
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63984727T= , CM000668.2:g.63984727T= GRCh38
NC_000006.11:g.64694620T= , CM000668.1:g.64694620T= GRCh37
NC_000006.10:g.64752579T= NCBI36
NG_023443.1:g.1727499A=
NG_023443.2:g.1727499A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6835-124A= MANE Select ENSP00000424243.1:n.6835-124A=
ENST00000370616.6:c.6835-124A= ENSP00000359650.2:n.6835-124A=
ENST00000370618.7:c.6835-124A= ENSP00000359652.4:n.6835-124A=
ENST00000370621.7:c.6835-124A= ENSP00000359655.3:n.6835-124A=
ENST00000398580.3:c.149-124A=
ENST00000503581.5:c.6835-124A= ENSP00000424243.1:n.6835-124A=
NM_001142800.1:c.6835-124A= NP_001136272.1:n.6835-124A=
NM_001292009.1:c.6835-124A= NP_001278938.1:n.6835-124A=
XR_001744188.1:n.606+16443T=
XR_001744189.1:n.129+16443T=
XR_001744190.1:n.197+16443T=
XR_001744191.1:n.607-927T=
NM_001142800.2:c.6835-124A= MANE Select NP_001136272.1:n.6835-124A=
NM_001292009.2:c.6835-124A= NP_001278938.1:n.6835-124A=