Canonical Allele Identifier: CA1633626745

Gene: EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230912_64230914delinsAAG , CM000668.2:g.64230912_64230914delinsAAG	GRCh38
NC_000006.11:g.64940805_64940807delinsAAG , CM000668.1:g.64940805_64940807delinsAAG	GRCh37
NC_000006.10:g.64998764_64998766delinsAAG	NCBI36
NG_023443.1:g.1481312_1481314delinsCTT
NG_023443.2:g.1481312_1481314delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6192-90_6192-88delinsCTT MANE Select	ENSP00000424243.1:n.6192-90_6192-88delinsCTT
ENST00000370616.6:c.6192-90_6192-88delinsCTT	ENSP00000359650.2:n.6192-90_6192-88delinsCTT
ENST00000370618.7:c.6192-90_6192-88delinsCTT	ENSP00000359652.4:n.6192-90_6192-88delinsCTT
ENST00000370621.7:c.6192-90_6192-88delinsCTT	ENSP00000359655.3:n.6192-90_6192-88delinsCTT
ENST00000503581.5:c.6192-90_6192-88delinsCTT	ENSP00000424243.1:n.6192-90_6192-88delinsCTT
NM_001142800.1:c.6192-90_6192-88delinsCTT	NP_001136272.1:n.6192-90_6192-88delinsCTT
NM_001292009.1:c.6192-90_6192-88delinsCTT	NP_001278938.1:n.6192-90_6192-88delinsCTT
NM_001142800.2:c.6192-90_6192-88delinsCTT MANE Select	NP_001136272.1:n.6192-90_6192-88delinsCTT
NM_001292009.2:c.6192-90_6192-88delinsCTT	NP_001278938.1:n.6192-90_6192-88delinsCTT