Canonical Allele Identifier: CA364388570

Gene: EYS

Linked Data

• MyVariant Identifiers: chr6:g.64694365G>C (hg19) ; chr6:g.63984472G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63984472G>C , CM000668.2:g.63984472G>C	GRCh38
NC_000006.11:g.64694365G>C , CM000668.1:g.64694365G>C	GRCh37
NC_000006.10:g.64752324G>C	NCBI36
NG_023443.1:g.1727754C>G
NG_023443.2:g.1727754C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000503581.6:c.6966C>G MANE Select	ENSP00000424243.1:p.Ile2322Met
ENST00000370616.6:c.6966C>G	ENSP00000359650.2:p.Ile2322Met
ENST00000370618.7:c.6966C>G	ENSP00000359652.4:p.Ile2322Met
ENST00000370621.7:c.6966C>G	ENSP00000359655.3:p.Ile2322Met
ENST00000398580.3:c.280C>G
ENST00000503581.5:c.6966C>G	ENSP00000424243.1:p.Ile2322Met
NM_001142800.1:c.6966C>G	NP_001136272.1:p.Ile2322Met
NM_001292009.1:c.6966C>G	NP_001278938.1:p.Ile2322Met
XR_001744188.1:n.606+16188G>C
XR_001744189.1:n.129+16188G>C
XR_001744190.1:n.197+16188G>C
XR_001744191.1:n.607-1182G>C
NM_001142800.2:c.6966C>G MANE Select	NP_001136272.1:p.Ile2322Met
NM_001292009.2:c.6966C>G	NP_001278938.1:p.Ile2322Met