Canonical Allele Identifier: CA1672406172
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398975C= , CM000668.2:g.150398975C= GRCh38
NC_000006.11:g.150720111C= , CM000668.1:g.150720111C= GRCh37
NC_000006.10:g.150761804C= NCBI36
NG_016007.1:g.35084C=
NG_016007.2:g.35084C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*738C= MANE Select ENSP00000343763.4:n.*738C=
ENST00000229447.9:c.*838C= ENSP00000229447.5:n.*838C=
ENST00000344419.7:c.*738C= ENSP00000343763.3:n.*738C=
NM_001164694.1:c.*838C= NP_001158166.1:n.*838C=
NM_001164695.1:c.*925C= NP_001158167.1:n.*925C=
NM_203395.2:c.*738C= NP_981932.1:n.*738C=
NM_001318495.1:c.*738C= NP_001305424.1:n.*738C=
NR_134655.1:n.1921C=
NM_001164694.2:c.*838C= NP_001158166.1:n.*838C=
NM_001164695.2:c.*925C= NP_001158167.1:n.*925C=
NM_001318495.2:c.*738C= NP_001305424.1:n.*738C=
NM_203395.3:c.*738C= MANE Select NP_981932.1:n.*738C=
NR_134655.2:n.1801C=