Canonical Allele Identifier: CA2771469888

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230905_64230912del , CM000668.2:g.64230905_64230912del	GRCh38
NC_000006.11:g.64940798_64940805del , CM000668.1:g.64940798_64940805del	GRCh37
NC_000006.10:g.64998757_64998764del	NCBI36
NG_023443.1:g.1481314_1481321del
NG_023443.2:g.1481314_1481321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6192-88_6192-81del MANE Select	ENSP00000424243.1:n.6192-88_6192-81del
ENST00000370616.6:c.6192-88_6192-81del	ENSP00000359650.2:n.6192-88_6192-81del
ENST00000370618.7:c.6192-88_6192-81del	ENSP00000359652.4:n.6192-88_6192-81del
ENST00000370621.7:c.6192-88_6192-81del	ENSP00000359655.3:n.6192-88_6192-81del
ENST00000503581.5:c.6192-88_6192-81del	ENSP00000424243.1:n.6192-88_6192-81del
NM_001142800.1:c.6192-88_6192-81del	NP_001136272.1:n.6192-88_6192-81del
NM_001292009.1:c.6192-88_6192-81del	NP_001278938.1:n.6192-88_6192-81del
NM_001142800.2:c.6192-88_6192-81del MANE Select	NP_001136272.1:n.6192-88_6192-81del
NM_001292009.2:c.6192-88_6192-81del	NP_001278938.1:n.6192-88_6192-81del