Canonical Allele Identifier: CA1672406017
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398659C= , CM000668.2:g.150398659C= GRCh38
NC_000006.11:g.150719795C= , CM000668.1:g.150719795C= GRCh37
NC_000006.10:g.150761488C= NCBI36
NG_016007.1:g.34768C=
NG_016007.2:g.34768C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*422C= MANE Select ENSP00000343763.4:n.*422C=
ENST00000229447.9:c.*522C= ENSP00000229447.5:n.*522C=
ENST00000344419.7:c.*422C= ENSP00000343763.3:n.*422C=
NM_001164694.1:c.*522C= NP_001158166.1:n.*522C=
NM_001164695.1:c.*609C= NP_001158167.1:n.*609C=
NM_203395.2:c.*422C= NP_981932.1:n.*422C=
NM_001318495.1:c.*422C= NP_001305424.1:n.*422C=
NR_134655.1:n.1605C=
NM_001164694.2:c.*522C= NP_001158166.1:n.*522C=
NM_001164695.2:c.*609C= NP_001158167.1:n.*609C=
NM_001318495.2:c.*422C= NP_001305424.1:n.*422C=
NM_203395.3:c.*422C= MANE Select NP_981932.1:n.*422C=
NR_134655.2:n.1485C=