Canonical Allele Identifier: CA2679283468

Gene: EYS

Linked Data

• gnomAD v4: 6-64230718-G-GTGCTGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230719_64230725dup , CM000668.2:g.64230719_64230725dup	GRCh38
NC_000006.11:g.64940612_64940618dup , CM000668.1:g.64940612_64940618dup	GRCh37
NC_000006.10:g.64998571_64998577dup	NCBI36
NG_023443.1:g.1481501_1481507dup
NG_023443.2:g.1481501_1481507dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6291_6297dup MANE Select	ENSP00000424243.1:p.Pro2100CysfsTer32
ENST00000370616.6:c.6291_6297dup	ENSP00000359650.2:p.Pro2100CysfsTer32
ENST00000370618.7:c.6291_6297dup	ENSP00000359652.4:p.Pro2100CysfsTer32
ENST00000370621.7:c.6291_6297dup	ENSP00000359655.3:p.Pro2100CysfsTer32
ENST00000503581.5:c.6291_6297dup	ENSP00000424243.1:p.Pro2100CysfsTer32
NM_001142800.1:c.6291_6297dup	NP_001136272.1:p.Pro2100CysfsTer32
NM_001292009.1:c.6291_6297dup	NP_001278938.1:p.Pro2100CysfsTer32
NM_001142800.2:c.6291_6297dup MANE Select	NP_001136272.1:p.Pro2100CysfsTer32
NM_001292009.2:c.6291_6297dup	NP_001278938.1:p.Pro2100CysfsTer32