Canonical Allele Identifier: CA1672406251
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399145C= , CM000668.2:g.150399145C= GRCh38
NC_000006.11:g.150720281C= , CM000668.1:g.150720281C= GRCh37
NC_000006.10:g.150761974C= NCBI36
NG_016007.1:g.35254C=
NG_016007.2:g.35254C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*908C= MANE Select ENSP00000343763.4:n.*908C=
ENST00000229447.9:c.*1008C= ENSP00000229447.5:n.*1008C=
ENST00000344419.7:c.*908C= ENSP00000343763.3:n.*908C=
NM_001164694.1:c.*1008C= NP_001158166.1:n.*1008C=
NM_001164695.1:c.*1095C= NP_001158167.1:n.*1095C=
NM_203395.2:c.*908C= NP_981932.1:n.*908C=
NM_001318495.1:c.*908C= NP_001305424.1:n.*908C=
NR_134655.1:n.2091C=
NM_001164694.2:c.*1008C= NP_001158166.1:n.*1008C=
NM_001164695.2:c.*1095C= NP_001158167.1:n.*1095C=
NM_001318495.2:c.*908C= NP_001305424.1:n.*908C=
NM_203395.3:c.*908C= MANE Select NP_981932.1:n.*908C=
NR_134655.2:n.1971C=