Canonical Allele Identifier: CA1672406226
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399100C= , CM000668.2:g.150399100C= GRCh38
NC_000006.11:g.150720236C= , CM000668.1:g.150720236C= GRCh37
NC_000006.10:g.150761929C= NCBI36
NG_016007.1:g.35209C=
NG_016007.2:g.35209C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*863C= MANE Select ENSP00000343763.4:n.*863C=
ENST00000229447.9:c.*963C= ENSP00000229447.5:n.*963C=
ENST00000344419.7:c.*863C= ENSP00000343763.3:n.*863C=
NM_001164694.1:c.*963C= NP_001158166.1:n.*963C=
NM_001164695.1:c.*1050C= NP_001158167.1:n.*1050C=
NM_203395.2:c.*863C= NP_981932.1:n.*863C=
NM_001318495.1:c.*863C= NP_001305424.1:n.*863C=
NR_134655.1:n.2046C=
NM_001164694.2:c.*963C= NP_001158166.1:n.*963C=
NM_001164695.2:c.*1050C= NP_001158167.1:n.*1050C=
NM_001318495.2:c.*863C= NP_001305424.1:n.*863C=
NM_203395.3:c.*863C= MANE Select NP_981932.1:n.*863C=
NR_134655.2:n.1926C=