Canonical Allele Identifier: CA1095800447

Gene: IYD

Linked Data

• dbSNP Id: rs1778429988
• gnomAD v3: 6-150399134-G-A
• gnomAD v4: 6-150399134-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399134G>A , CM000668.2:g.150399134G>A	GRCh38
NC_000006.11:g.150720270G>A , CM000668.1:g.150720270G>A	GRCh37
NC_000006.10:g.150761963G>A	NCBI36
NG_016007.1:g.35243G>A
NG_016007.2:g.35243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*897G>A MANE Select	ENSP00000343763.4:n.*897G>A
ENST00000229447.9:c.*997G>A	ENSP00000229447.5:n.*997G>A
ENST00000344419.7:c.*897G>A	ENSP00000343763.3:n.*897G>A
NM_001164694.1:c.*997G>A	NP_001158166.1:n.*997G>A
NM_001164695.1:c.*1084G>A	NP_001158167.1:n.*1084G>A
NM_203395.2:c.*897G>A	NP_981932.1:n.*897G>A
NM_001318495.1:c.*897G>A	NP_001305424.1:n.*897G>A
NR_134655.1:n.2080G>A
NM_001164694.2:c.*997G>A	NP_001158166.1:n.*997G>A
NM_001164695.2:c.*1084G>A	NP_001158167.1:n.*1084G>A
NM_001318495.2:c.*897G>A	NP_001305424.1:n.*897G>A
NM_203395.3:c.*897G>A MANE Select	NP_981932.1:n.*897G>A
NR_134655.2:n.1960G>A