Canonical Allele Identifier: CA1672406103

Gene: IYD

Linked Data

• dbSNP Id: rs1778421716
• gnomAD v4: 6-150398823-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398823C>A , CM000668.2:g.150398823C>A	GRCh38
NC_000006.11:g.150719959C>A , CM000668.1:g.150719959C>A	GRCh37
NC_000006.10:g.150761652C>A	NCBI36
NG_016007.1:g.34932C>A
NG_016007.2:g.34932C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*586C>A MANE Select	ENSP00000343763.4:n.*586C>A
ENST00000229447.9:c.*686C>A	ENSP00000229447.5:n.*686C>A
ENST00000344419.7:c.*586C>A	ENSP00000343763.3:n.*586C>A
NM_001164694.1:c.*686C>A	NP_001158166.1:n.*686C>A
NM_001164695.1:c.*773C>A	NP_001158167.1:n.*773C>A
NM_203395.2:c.*586C>A	NP_981932.1:n.*586C>A
NM_001318495.1:c.*586C>A	NP_001305424.1:n.*586C>A
NR_134655.1:n.1769C>A
NM_001164694.2:c.*686C>A	NP_001158166.1:n.*686C>A
NM_001164695.2:c.*773C>A	NP_001158167.1:n.*773C>A
NM_001318495.2:c.*586C>A	NP_001305424.1:n.*586C>A
NM_203395.3:c.*586C>A MANE Select	NP_981932.1:n.*586C>A
NR_134655.2:n.1649C>A