Canonical Allele Identifier: CA1672406232
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399108C= , CM000668.2:g.150399108C= GRCh38
NC_000006.11:g.150720244C= , CM000668.1:g.150720244C= GRCh37
NC_000006.10:g.150761937C= NCBI36
NG_016007.1:g.35217C=
NG_016007.2:g.35217C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*871C= MANE Select ENSP00000343763.4:n.*871C=
ENST00000229447.9:c.*971C= ENSP00000229447.5:n.*971C=
ENST00000344419.7:c.*871C= ENSP00000343763.3:n.*871C=
NM_001164694.1:c.*971C= NP_001158166.1:n.*971C=
NM_001164695.1:c.*1058C= NP_001158167.1:n.*1058C=
NM_203395.2:c.*871C= NP_981932.1:n.*871C=
NM_001318495.1:c.*871C= NP_001305424.1:n.*871C=
NR_134655.1:n.2054C=
NM_001164694.2:c.*971C= NP_001158166.1:n.*971C=
NM_001164695.2:c.*1058C= NP_001158167.1:n.*1058C=
NM_001318495.2:c.*871C= NP_001305424.1:n.*871C=
NM_203395.3:c.*871C= MANE Select NP_981932.1:n.*871C=
NR_134655.2:n.1934C=