Canonical Allele Identifier: CA1672406227
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399101C= , CM000668.2:g.150399101C= GRCh38
NC_000006.11:g.150720237C= , CM000668.1:g.150720237C= GRCh37
NC_000006.10:g.150761930C= NCBI36
NG_016007.1:g.35210C=
NG_016007.2:g.35210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*864C= MANE Select ENSP00000343763.4:n.*864C=
ENST00000229447.9:c.*964C= ENSP00000229447.5:n.*964C=
ENST00000344419.7:c.*864C= ENSP00000343763.3:n.*864C=
NM_001164694.1:c.*964C= NP_001158166.1:n.*964C=
NM_001164695.1:c.*1051C= NP_001158167.1:n.*1051C=
NM_203395.2:c.*864C= NP_981932.1:n.*864C=
NM_001318495.1:c.*864C= NP_001305424.1:n.*864C=
NR_134655.1:n.2047C=
NM_001164694.2:c.*964C= NP_001158166.1:n.*964C=
NM_001164695.2:c.*1051C= NP_001158167.1:n.*1051C=
NM_001318495.2:c.*864C= NP_001305424.1:n.*864C=
NM_203395.3:c.*864C= MANE Select NP_981932.1:n.*864C=
NR_134655.2:n.1927C=