Canonical Allele Identifier: CA1672406021
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398669C= , CM000668.2:g.150398669C= GRCh38
NC_000006.11:g.150719805C= , CM000668.1:g.150719805C= GRCh37
NC_000006.10:g.150761498C= NCBI36
NG_016007.1:g.34778C=
NG_016007.2:g.34778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*432C= MANE Select ENSP00000343763.4:n.*432C=
ENST00000229447.9:c.*532C= ENSP00000229447.5:n.*532C=
ENST00000344419.7:c.*432C= ENSP00000343763.3:n.*432C=
NM_001164694.1:c.*532C= NP_001158166.1:n.*532C=
NM_001164695.1:c.*619C= NP_001158167.1:n.*619C=
NM_203395.2:c.*432C= NP_981932.1:n.*432C=
NM_001318495.1:c.*432C= NP_001305424.1:n.*432C=
NR_134655.1:n.1615C=
NM_001164694.2:c.*532C= NP_001158166.1:n.*532C=
NM_001164695.2:c.*619C= NP_001158167.1:n.*619C=
NM_001318495.2:c.*432C= NP_001305424.1:n.*432C=
NM_203395.3:c.*432C= MANE Select NP_981932.1:n.*432C=
NR_134655.2:n.1495C=