Canonical Allele Identifier: CA366030676
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389499A>C , CM000668.2:g.150389499A>C GRCh38
NC_000006.11:g.150710635A>C , CM000668.1:g.150710635A>C GRCh37
NC_000006.10:g.150752328A>C NCBI36
NG_016007.1:g.25608A>C
NG_016007.2:g.25608A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.326A>C MANE Select ENSP00000343763.4:p.Glu109Ala
ENST00000229447.9:c.326A>C ENSP00000229447.5:p.Glu109Ala
ENST00000344419.7:c.326A>C ENSP00000343763.3:p.Glu109Ala
ENST00000367335.7:c.326A>C ENSP00000356304.3:p.Glu109Ala
ENST00000392255.7:c.326A>C ENSP00000376084.3:p.Glu109Ala
ENST00000392256.6:c.326A>C ENSP00000376085.2:p.Glu109Ala
ENST00000422583.2:c.179+24A>C ENSP00000397342.2:n.179+24A>C
ENST00000425615.3:c.161A>C ENSP00000390081.3:p.Glu54Ala
ENST00000500320.7:c.326A>C ENSP00000441276.1:p.Glu109Ala
ENST00000546121.1:n.269A>C
NM_001164694.1:c.326A>C NP_001158166.1:p.Glu109Ala
NM_001164695.1:c.326A>C NP_001158167.1:p.Glu109Ala
NM_203395.2:c.326A>C NP_981932.1:p.Glu109Ala
XM_006715478.2:c.326A>C XP_006715541.1:p.Glu109Ala
XM_006715479.2:c.161A>C XP_006715542.1:p.Glu54Ala
XR_245516.3:n.489A>C
NM_001318495.1:c.124+24A>C NP_001305424.1:n.124+24A>C
NR_134655.1:n.466A>C
XM_006715478.3:c.326A>C XP_006715541.1:p.Glu109Ala
XM_006715479.3:c.161A>C XP_006715542.1:p.Glu54Ala
NM_001164694.2:c.326A>C NP_001158166.1:p.Glu109Ala
NM_001164695.2:c.326A>C NP_001158167.1:p.Glu109Ala
NM_001318495.2:c.124+24A>C NP_001305424.1:n.124+24A>C
NM_203395.3:c.326A>C MANE Select NP_981932.1:p.Glu109Ala
NR_134655.2:n.346A>C