Canonical Allele Identifier: CA1672406075
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398784G= , CM000668.2:g.150398784G= GRCh38
NC_000006.11:g.150719920G= , CM000668.1:g.150719920G= GRCh37
NC_000006.10:g.150761613G= NCBI36
NG_016007.1:g.34893G=
NG_016007.2:g.34893G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*547G= MANE Select ENSP00000343763.4:n.*547G=
ENST00000229447.9:c.*647G= ENSP00000229447.5:n.*647G=
ENST00000344419.7:c.*547G= ENSP00000343763.3:n.*547G=
NM_001164694.1:c.*647G= NP_001158166.1:n.*647G=
NM_001164695.1:c.*734G= NP_001158167.1:n.*734G=
NM_203395.2:c.*547G= NP_981932.1:n.*547G=
NM_001318495.1:c.*547G= NP_001305424.1:n.*547G=
NR_134655.1:n.1730G=
NM_001164694.2:c.*647G= NP_001158166.1:n.*647G=
NM_001164695.2:c.*734G= NP_001158167.1:n.*734G=
NM_001318495.2:c.*547G= NP_001305424.1:n.*547G=
NM_203395.3:c.*547G= MANE Select NP_981932.1:n.*547G=
NR_134655.2:n.1610G=