Canonical Allele Identifier: CA364389008

Gene: EYS

Linked Data

• gnomAD v4: 6-63984569-G-T
• MyVariant Identifiers: chr6:g.64694462G>T (hg19) ; chr6:g.63984569G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984569G>T , CM000668.2:g.63984569G>T	GRCh38
NC_000006.11:g.64694462G>T , CM000668.1:g.64694462G>T	GRCh37
NC_000006.10:g.64752421G>T	NCBI36
NG_023443.1:g.1727657C>A
NG_023443.2:g.1727657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6869C>A MANE Select	ENSP00000424243.1:p.Pro2290His
ENST00000370616.6:c.6869C>A	ENSP00000359650.2:p.Pro2290His
ENST00000370618.7:c.6869C>A	ENSP00000359652.4:p.Pro2290His
ENST00000370621.7:c.6869C>A	ENSP00000359655.3:p.Pro2290His
ENST00000398580.3:c.183C>A
ENST00000503581.5:c.6869C>A	ENSP00000424243.1:p.Pro2290His
NM_001142800.1:c.6869C>A	NP_001136272.1:p.Pro2290His
NM_001292009.1:c.6869C>A	NP_001278938.1:p.Pro2290His
XR_001744188.1:n.606+16285G>T
XR_001744189.1:n.129+16285G>T
XR_001744190.1:n.197+16285G>T
XR_001744191.1:n.607-1085G>T
NM_001142800.2:c.6869C>A MANE Select	NP_001136272.1:p.Pro2290His
NM_001292009.2:c.6869C>A	NP_001278938.1:p.Pro2290His