Canonical Allele Identifier: CA1672406002
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398611T= , CM000668.2:g.150398611T= GRCh38
NC_000006.11:g.150719747T= , CM000668.1:g.150719747T= GRCh37
NC_000006.10:g.150761440T= NCBI36
NG_016007.1:g.34720T=
NG_016007.2:g.34720T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*374T= MANE Select ENSP00000343763.4:n.*374T=
ENST00000229447.9:c.*474T= ENSP00000229447.5:n.*474T=
ENST00000344419.7:c.*374T= ENSP00000343763.3:n.*374T=
NM_001164694.1:c.*474T= NP_001158166.1:n.*474T=
NM_001164695.1:c.*561T= NP_001158167.1:n.*561T=
NM_203395.2:c.*374T= NP_981932.1:n.*374T=
NM_001318495.1:c.*374T= NP_001305424.1:n.*374T=
NR_134655.1:n.1557T=
NM_001164694.2:c.*474T= NP_001158166.1:n.*474T=
NM_001164695.2:c.*561T= NP_001158167.1:n.*561T=
NM_001318495.2:c.*374T= NP_001305424.1:n.*374T=
NM_203395.3:c.*374T= MANE Select NP_981932.1:n.*374T=
NR_134655.2:n.1437T=