Canonical Allele Identifier: CA2771469860

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230877_64230879del , CM000668.2:g.64230877_64230879del	GRCh38
NC_000006.11:g.64940770_64940772del , CM000668.1:g.64940770_64940772del	GRCh37
NC_000006.10:g.64998729_64998731del	NCBI36
NG_023443.1:g.1481347_1481349del
NG_023443.2:g.1481347_1481349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6192-55_6192-53del MANE Select	ENSP00000424243.1:n.6192-55_6192-53del
ENST00000370616.6:c.6192-55_6192-53del	ENSP00000359650.2:n.6192-55_6192-53del
ENST00000370618.7:c.6192-55_6192-53del	ENSP00000359652.4:n.6192-55_6192-53del
ENST00000370621.7:c.6192-55_6192-53del	ENSP00000359655.3:n.6192-55_6192-53del
ENST00000503581.5:c.6192-55_6192-53del	ENSP00000424243.1:n.6192-55_6192-53del
NM_001142800.1:c.6192-55_6192-53del	NP_001136272.1:n.6192-55_6192-53del
NM_001292009.1:c.6192-55_6192-53del	NP_001278938.1:n.6192-55_6192-53del
NM_001142800.2:c.6192-55_6192-53del MANE Select	NP_001136272.1:n.6192-55_6192-53del
NM_001292009.2:c.6192-55_6192-53del	NP_001278938.1:n.6192-55_6192-53del