Canonical Allele Identifier: CA2680762477

Gene: IYD

Linked Data

• gnomAD v4: 6-150398766-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398766G>A , CM000668.2:g.150398766G>A	GRCh38
NC_000006.11:g.150719902G>A , CM000668.1:g.150719902G>A	GRCh37
NC_000006.10:g.150761595G>A	NCBI36
NG_016007.1:g.34875G>A
NG_016007.2:g.34875G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*529G>A MANE Select	ENSP00000343763.4:n.*529G>A
ENST00000229447.9:c.*629G>A	ENSP00000229447.5:n.*629G>A
ENST00000344419.7:c.*529G>A	ENSP00000343763.3:n.*529G>A
NM_001164694.1:c.*629G>A	NP_001158166.1:n.*629G>A
NM_001164695.1:c.*716G>A	NP_001158167.1:n.*716G>A
NM_203395.2:c.*529G>A	NP_981932.1:n.*529G>A
NM_001318495.1:c.*529G>A	NP_001305424.1:n.*529G>A
NR_134655.1:n.1712G>A
NM_001164694.2:c.*629G>A	NP_001158166.1:n.*629G>A
NM_001164695.2:c.*716G>A	NP_001158167.1:n.*716G>A
NM_001318495.2:c.*529G>A	NP_001305424.1:n.*529G>A
NM_203395.3:c.*529G>A MANE Select	NP_981932.1:n.*529G>A
NR_134655.2:n.1592G>A