Canonical Allele Identifier: CA364790630
Community Standard Title: NM_001142800.2(EYS):c.110C>A (p.Ser37Ter)
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.65495301G>T , CM000668.2:g.65495301G>T GRCh38
NC_000006.11:g.66205194G>T , CM000668.1:g.66205194G>T GRCh37
NC_000006.10:g.66261915G>T NCBI36
NG_023443.1:g.216925C>A
NG_023443.2:g.216925C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.110C>A MANE Select NP_001136272.1:p.Ser37Ter
ENST00000503581.6:c.110C>A MANE Select ENSP00000424243.1:p.Ser37Ter
NM_001142800.1:c.110C>A NP_001136272.1:p.Ser37Ter
NM_001142801.1:c.110C>A NP_001136273.1:p.Ser37Ter
NM_001142801.2:c.110C>A NP_001136273.1:p.Ser37Ter
NM_001292009.1:c.110C>A NP_001278938.1:p.Ser37Ter
NM_001292009.2:c.110C>A NP_001278938.1:p.Ser37Ter
NM_198283.1:c.110C>A NP_938024.1:p.Ser37Ter
NM_198283.2:c.110C>A NP_938024.1:p.Ser37Ter
ENST00000342421.9:c.110C>A ENSP00000341818.5:p.Ser37Ter
ENST00000370616.6:c.110C>A ENSP00000359650.2:p.Ser37Ter
ENST00000370618.7:c.110C>A ENSP00000359652.4:p.Ser37Ter
ENST00000370621.7:c.110C>A ENSP00000359655.3:p.Ser37Ter
ENST00000393380.6:c.110C>A ENSP00000377042.2:p.Ser37Ter
ENST00000471279.1:c.-200C>A ENSP00000420530.1:n.-200C>A
ENST00000489873.1:n.637C>A
ENST00000503581.5:c.110C>A ENSP00000424243.1:p.Ser37Ter