Canonical Allele Identifier: CA1672406230
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399105G= , CM000668.2:g.150399105G= GRCh38
NC_000006.11:g.150720241G= , CM000668.1:g.150720241G= GRCh37
NC_000006.10:g.150761934G= NCBI36
NG_016007.1:g.35214G=
NG_016007.2:g.35214G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*868G= MANE Select ENSP00000343763.4:n.*868G=
ENST00000229447.9:c.*968G= ENSP00000229447.5:n.*968G=
ENST00000344419.7:c.*868G= ENSP00000343763.3:n.*868G=
NM_001164694.1:c.*968G= NP_001158166.1:n.*968G=
NM_001164695.1:c.*1055G= NP_001158167.1:n.*1055G=
NM_203395.2:c.*868G= NP_981932.1:n.*868G=
NM_001318495.1:c.*868G= NP_001305424.1:n.*868G=
NR_134655.1:n.2051G=
NM_001164694.2:c.*968G= NP_001158166.1:n.*968G=
NM_001164695.2:c.*1055G= NP_001158167.1:n.*1055G=
NM_001318495.2:c.*868G= NP_001305424.1:n.*868G=
NM_203395.3:c.*868G= MANE Select NP_981932.1:n.*868G=
NR_134655.2:n.1931G=