Canonical Allele Identifier: CA1672406205
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399042C= , CM000668.2:g.150399042C= GRCh38
NC_000006.11:g.150720178C= , CM000668.1:g.150720178C= GRCh37
NC_000006.10:g.150761871C= NCBI36
NG_016007.1:g.35151C=
NG_016007.2:g.35151C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*805C= MANE Select ENSP00000343763.4:n.*805C=
ENST00000229447.9:c.*905C= ENSP00000229447.5:n.*905C=
ENST00000344419.7:c.*805C= ENSP00000343763.3:n.*805C=
NM_001164694.1:c.*905C= NP_001158166.1:n.*905C=
NM_001164695.1:c.*992C= NP_001158167.1:n.*992C=
NM_203395.2:c.*805C= NP_981932.1:n.*805C=
NM_001318495.1:c.*805C= NP_001305424.1:n.*805C=
NR_134655.1:n.1988C=
NM_001164694.2:c.*905C= NP_001158166.1:n.*905C=
NM_001164695.2:c.*992C= NP_001158167.1:n.*992C=
NM_001318495.2:c.*805C= NP_001305424.1:n.*805C=
NM_203395.3:c.*805C= MANE Select NP_981932.1:n.*805C=
NR_134655.2:n.1868C=