Canonical Allele Identifier: CA1672406180
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399001C= , CM000668.2:g.150399001C= GRCh38
NC_000006.11:g.150720137C= , CM000668.1:g.150720137C= GRCh37
NC_000006.10:g.150761830C= NCBI36
NG_016007.1:g.35110C=
NG_016007.2:g.35110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*764C= MANE Select ENSP00000343763.4:n.*764C=
ENST00000229447.9:c.*864C= ENSP00000229447.5:n.*864C=
ENST00000344419.7:c.*764C= ENSP00000343763.3:n.*764C=
NM_001164694.1:c.*864C= NP_001158166.1:n.*864C=
NM_001164695.1:c.*951C= NP_001158167.1:n.*951C=
NM_203395.2:c.*764C= NP_981932.1:n.*764C=
NM_001318495.1:c.*764C= NP_001305424.1:n.*764C=
NR_134655.1:n.1947C=
NM_001164694.2:c.*864C= NP_001158166.1:n.*864C=
NM_001164695.2:c.*951C= NP_001158167.1:n.*951C=
NM_001318495.2:c.*764C= NP_001305424.1:n.*764C=
NM_203395.3:c.*764C= MANE Select NP_981932.1:n.*764C=
NR_134655.2:n.1827C=