Canonical Allele Identifier: CA2680762918

Gene: IYD

Linked Data

• gnomAD v4: 6-150399128-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399128G>A , CM000668.2:g.150399128G>A	GRCh38
NC_000006.11:g.150720264G>A , CM000668.1:g.150720264G>A	GRCh37
NC_000006.10:g.150761957G>A	NCBI36
NG_016007.1:g.35237G>A
NG_016007.2:g.35237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*891G>A MANE Select	ENSP00000343763.4:n.*891G>A
ENST00000229447.9:c.*991G>A	ENSP00000229447.5:n.*991G>A
ENST00000344419.7:c.*891G>A	ENSP00000343763.3:n.*891G>A
NM_001164694.1:c.*991G>A	NP_001158166.1:n.*991G>A
NM_001164695.1:c.*1078G>A	NP_001158167.1:n.*1078G>A
NM_203395.2:c.*891G>A	NP_981932.1:n.*891G>A
NM_001318495.1:c.*891G>A	NP_001305424.1:n.*891G>A
NR_134655.1:n.2074G>A
NM_001164694.2:c.*991G>A	NP_001158166.1:n.*991G>A
NM_001164695.2:c.*1078G>A	NP_001158167.1:n.*1078G>A
NM_001318495.2:c.*891G>A	NP_001305424.1:n.*891G>A
NM_203395.3:c.*891G>A MANE Select	NP_981932.1:n.*891G>A
NR_134655.2:n.1954G>A