Canonical Allele Identifier: CA1672401668
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389441T= , CM000668.2:g.150389441T= GRCh38
NC_000006.11:g.150710577T= , CM000668.1:g.150710577T= GRCh37
NC_000006.10:g.150752270T= NCBI36
NG_016007.1:g.25550T=
NG_016007.2:g.25550T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.268T= MANE Select ENSP00000343763.4:p.Ser90=
ENST00000229447.9:c.268T= ENSP00000229447.5:p.Ser90=
ENST00000344419.7:c.268T= ENSP00000343763.3:p.Ser90=
ENST00000367335.7:c.268T= ENSP00000356304.3:p.Ser90=
ENST00000392255.7:c.268T= ENSP00000376084.3:p.Ser90=
ENST00000392256.6:c.268T= ENSP00000376085.2:p.Ser90=
ENST00000422583.2:c.145T= ENSP00000397342.2:p.Ser49=
ENST00000425615.3:c.103T= ENSP00000390081.3:p.Ser35=
ENST00000500320.7:c.268T= ENSP00000441276.1:p.Ser90=
ENST00000546121.1:n.211T=
NM_001164694.1:c.268T= NP_001158166.1:p.Ser90=
NM_001164695.1:c.268T= NP_001158167.1:p.Ser90=
NM_203395.2:c.268T= NP_981932.1:p.Ser90=
XM_006715478.2:c.268T= XP_006715541.1:p.Ser90=
XM_006715479.2:c.103T= XP_006715542.1:p.Ser35=
XR_245516.3:n.431T=
NM_001318495.1:c.90T= NP_001305424.1:p.Gly30=
NR_134655.1:n.408T=
XM_006715478.3:c.268T= XP_006715541.1:p.Ser90=
XM_006715479.3:c.103T= XP_006715542.1:p.Ser35=
NM_001164694.2:c.268T= NP_001158166.1:p.Ser90=
NM_001164695.2:c.268T= NP_001158167.1:p.Ser90=
NM_001318495.2:c.90T= NP_001305424.1:p.Gly30=
NM_203395.3:c.268T= MANE Select NP_981932.1:p.Ser90=
NR_134655.2:n.288T=