Canonical Allele Identifier: CA1672406231
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399106G= , CM000668.2:g.150399106G= GRCh38
NC_000006.11:g.150720242G= , CM000668.1:g.150720242G= GRCh37
NC_000006.10:g.150761935G= NCBI36
NG_016007.1:g.35215G=
NG_016007.2:g.35215G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*869G= MANE Select ENSP00000343763.4:n.*869G=
ENST00000229447.9:c.*969G= ENSP00000229447.5:n.*969G=
ENST00000344419.7:c.*869G= ENSP00000343763.3:n.*869G=
NM_001164694.1:c.*969G= NP_001158166.1:n.*969G=
NM_001164695.1:c.*1056G= NP_001158167.1:n.*1056G=
NM_203395.2:c.*869G= NP_981932.1:n.*869G=
NM_001318495.1:c.*869G= NP_001305424.1:n.*869G=
NR_134655.1:n.2052G=
NM_001164694.2:c.*969G= NP_001158166.1:n.*969G=
NM_001164695.2:c.*1056G= NP_001158167.1:n.*1056G=
NM_001318495.2:c.*869G= NP_001305424.1:n.*869G=
NM_203395.3:c.*869G= MANE Select NP_981932.1:n.*869G=
NR_134655.2:n.1932G=