Canonical Allele Identifier: CA1672406037
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398696T= , CM000668.2:g.150398696T= GRCh38
NC_000006.11:g.150719832T= , CM000668.1:g.150719832T= GRCh37
NC_000006.10:g.150761525T= NCBI36
NG_016007.1:g.34805T=
NG_016007.2:g.34805T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*459T= MANE Select ENSP00000343763.4:n.*459T=
ENST00000229447.9:c.*559T= ENSP00000229447.5:n.*559T=
ENST00000344419.7:c.*459T= ENSP00000343763.3:n.*459T=
NM_001164694.1:c.*559T= NP_001158166.1:n.*559T=
NM_001164695.1:c.*646T= NP_001158167.1:n.*646T=
NM_203395.2:c.*459T= NP_981932.1:n.*459T=
NM_001318495.1:c.*459T= NP_001305424.1:n.*459T=
NR_134655.1:n.1642T=
NM_001164694.2:c.*559T= NP_001158166.1:n.*559T=
NM_001164695.2:c.*646T= NP_001158167.1:n.*646T=
NM_001318495.2:c.*459T= NP_001305424.1:n.*459T=
NM_203395.3:c.*459T= MANE Select NP_981932.1:n.*459T=
NR_134655.2:n.1522T=