Canonical Allele Identifier: CA1672406203
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399040C= , CM000668.2:g.150399040C= GRCh38
NC_000006.11:g.150720176C= , CM000668.1:g.150720176C= GRCh37
NC_000006.10:g.150761869C= NCBI36
NG_016007.1:g.35149C=
NG_016007.2:g.35149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*803C= MANE Select ENSP00000343763.4:n.*803C=
ENST00000229447.9:c.*903C= ENSP00000229447.5:n.*903C=
ENST00000344419.7:c.*803C= ENSP00000343763.3:n.*803C=
NM_001164694.1:c.*903C= NP_001158166.1:n.*903C=
NM_001164695.1:c.*990C= NP_001158167.1:n.*990C=
NM_203395.2:c.*803C= NP_981932.1:n.*803C=
NM_001318495.1:c.*803C= NP_001305424.1:n.*803C=
NR_134655.1:n.1986C=
NM_001164694.2:c.*903C= NP_001158166.1:n.*903C=
NM_001164695.2:c.*990C= NP_001158167.1:n.*990C=
NM_001318495.2:c.*803C= NP_001305424.1:n.*803C=
NM_203395.3:c.*803C= MANE Select NP_981932.1:n.*803C=
NR_134655.2:n.1866C=