Canonical Allele Identifier: CA2771459753

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788405_63788406insACA , CM000668.2:g.63788405_63788406insACA	GRCh38
NC_000006.11:g.64498298_64498299insACA , CM000668.1:g.64498298_64498299insACA	GRCh37
NC_000006.10:g.64556257_64556258insACA	NCBI36
NG_023443.1:g.1923820_1923821insTGT
NG_023443.2:g.1923820_1923821insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7579-157_7579-156insTGT MANE Select	ENSP00000424243.1:n.7579-157_7579-156insTGT
ENST00000370616.6:c.7579-157_7579-156insTGT	ENSP00000359650.2:n.7579-157_7579-156insTGT
ENST00000370618.7:c.7579-157_7579-156insTGT	ENSP00000359652.4:n.7579-157_7579-156insTGT
ENST00000370621.7:c.7579-157_7579-156insTGT	ENSP00000359655.3:n.7579-157_7579-156insTGT
ENST00000398580.3:c.893-157_893-156insTGT
ENST00000486069.1:n.219-157_219-156insTGT
ENST00000503581.5:c.7579-157_7579-156insTGT	ENSP00000424243.1:n.7579-157_7579-156insTGT
NM_001142800.1:c.7579-157_7579-156insTGT	NP_001136272.1:n.7579-157_7579-156insTGT
NM_001292009.1:c.7579-157_7579-156insTGT	NP_001278938.1:n.7579-157_7579-156insTGT
NM_001142800.2:c.7579-157_7579-156insTGT MANE Select	NP_001136272.1:n.7579-157_7579-156insTGT
NM_001292009.2:c.7579-157_7579-156insTGT	NP_001278938.1:n.7579-157_7579-156insTGT