Canonical Allele Identifier: CA1672406255
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399156T= , CM000668.2:g.150399156T= GRCh38
NC_000006.11:g.150720292T= , CM000668.1:g.150720292T= GRCh37
NC_000006.10:g.150761985T= NCBI36
NG_016007.1:g.35265T=
NG_016007.2:g.35265T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*919T= MANE Select ENSP00000343763.4:n.*919T=
ENST00000229447.9:c.*1019T= ENSP00000229447.5:n.*1019T=
ENST00000344419.7:c.*919T= ENSP00000343763.3:n.*919T=
NM_001164694.1:c.*1019T= NP_001158166.1:n.*1019T=
NM_001164695.1:c.*1106T= NP_001158167.1:n.*1106T=
NM_203395.2:c.*919T= NP_981932.1:n.*919T=
NM_001318495.1:c.*919T= NP_001305424.1:n.*919T=
NR_134655.1:n.2102T=
NM_001164694.2:c.*1019T= NP_001158166.1:n.*1019T=
NM_001164695.2:c.*1106T= NP_001158167.1:n.*1106T=
NM_001318495.2:c.*919T= NP_001305424.1:n.*919T=
NM_203395.3:c.*919T= MANE Select NP_981932.1:n.*919T=
NR_134655.2:n.1982T=