Canonical Allele Identifier: CA1672405993
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398597A= , CM000668.2:g.150398597A= GRCh38
NC_000006.11:g.150719733A= , CM000668.1:g.150719733A= GRCh37
NC_000006.10:g.150761426A= NCBI36
NG_016007.1:g.34706A=
NG_016007.2:g.34706A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*360A= MANE Select ENSP00000343763.4:n.*360A=
ENST00000229447.9:c.*460A= ENSP00000229447.5:n.*460A=
ENST00000344419.7:c.*360A= ENSP00000343763.3:n.*360A=
NM_001164694.1:c.*460A= NP_001158166.1:n.*460A=
NM_001164695.1:c.*547A= NP_001158167.1:n.*547A=
NM_203395.2:c.*360A= NP_981932.1:n.*360A=
NM_001318495.1:c.*360A= NP_001305424.1:n.*360A=
NR_134655.1:n.1543A=
NM_001164694.2:c.*460A= NP_001158166.1:n.*460A=
NM_001164695.2:c.*547A= NP_001158167.1:n.*547A=
NM_001318495.2:c.*360A= NP_001305424.1:n.*360A=
NM_203395.3:c.*360A= MANE Select NP_981932.1:n.*360A=
NR_134655.2:n.1423A=