Canonical Allele Identifier: CA2679283488

Gene: EYS

Linked Data

• gnomAD v4: 6-64230856-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230856T>G , CM000668.2:g.64230856T>G	GRCh38
NC_000006.11:g.64940749T>G , CM000668.1:g.64940749T>G	GRCh37
NC_000006.10:g.64998708T>G	NCBI36
NG_023443.1:g.1481370A>C
NG_023443.2:g.1481370A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6192-32A>C MANE Select	ENSP00000424243.1:n.6192-32A>C
ENST00000370616.6:c.6192-32A>C	ENSP00000359650.2:n.6192-32A>C
ENST00000370618.7:c.6192-32A>C	ENSP00000359652.4:n.6192-32A>C
ENST00000370621.7:c.6192-32A>C	ENSP00000359655.3:n.6192-32A>C
ENST00000503581.5:c.6192-32A>C	ENSP00000424243.1:n.6192-32A>C
NM_001142800.1:c.6192-32A>C	NP_001136272.1:n.6192-32A>C
NM_001292009.1:c.6192-32A>C	NP_001278938.1:n.6192-32A>C
NM_001142800.2:c.6192-32A>C MANE Select	NP_001136272.1:n.6192-32A>C
NM_001292009.2:c.6192-32A>C	NP_001278938.1:n.6192-32A>C