Canonical Allele Identifier: CA1672406114
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398847G= , CM000668.2:g.150398847G= GRCh38
NC_000006.11:g.150719983G= , CM000668.1:g.150719983G= GRCh37
NC_000006.10:g.150761676G= NCBI36
NG_016007.1:g.34956G=
NG_016007.2:g.34956G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*610G= MANE Select ENSP00000343763.4:n.*610G=
ENST00000229447.9:c.*710G= ENSP00000229447.5:n.*710G=
ENST00000344419.7:c.*610G= ENSP00000343763.3:n.*610G=
NM_001164694.1:c.*710G= NP_001158166.1:n.*710G=
NM_001164695.1:c.*797G= NP_001158167.1:n.*797G=
NM_203395.2:c.*610G= NP_981932.1:n.*610G=
NM_001318495.1:c.*610G= NP_001305424.1:n.*610G=
NR_134655.1:n.1793G=
NM_001164694.2:c.*710G= NP_001158166.1:n.*710G=
NM_001164695.2:c.*797G= NP_001158167.1:n.*797G=
NM_001318495.2:c.*610G= NP_001305424.1:n.*610G=
NM_203395.3:c.*610G= MANE Select NP_981932.1:n.*610G=
NR_134655.2:n.1673G=