Canonical Allele Identifier: CA1672406042
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398701C= , CM000668.2:g.150398701C= GRCh38
NC_000006.11:g.150719837C= , CM000668.1:g.150719837C= GRCh37
NC_000006.10:g.150761530C= NCBI36
NG_016007.1:g.34810C=
NG_016007.2:g.34810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*464C= MANE Select ENSP00000343763.4:n.*464C=
ENST00000229447.9:c.*564C= ENSP00000229447.5:n.*564C=
ENST00000344419.7:c.*464C= ENSP00000343763.3:n.*464C=
NM_001164694.1:c.*564C= NP_001158166.1:n.*564C=
NM_001164695.1:c.*651C= NP_001158167.1:n.*651C=
NM_203395.2:c.*464C= NP_981932.1:n.*464C=
NM_001318495.1:c.*464C= NP_001305424.1:n.*464C=
NR_134655.1:n.1647C=
NM_001164694.2:c.*564C= NP_001158166.1:n.*564C=
NM_001164695.2:c.*651C= NP_001158167.1:n.*651C=
NM_001318495.2:c.*464C= NP_001305424.1:n.*464C=
NM_203395.3:c.*464C= MANE Select NP_981932.1:n.*464C=
NR_134655.2:n.1527C=