Canonical Allele Identifier: CA2669475632
Gene: IDUA HGNC NCBI
SLC26A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.987356_987357insAGAGC , CM000666.2:g.987356_987357insAGAGC GRCh38
NC_000004.11:g.981144_981145insAGAGC , CM000666.1:g.981144_981145insAGAGC GRCh37
NC_000004.10:g.971144_971145insAGAGC NCBI36
NG_008103.1:g.5360_5361insAGAGC
NG_033042.1:g.11080_11081insGCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.158+114_158+115insAGAGC (IDUA) ENSP00000247933.4:n.158+114_158+115insAGAGC
ENST00000514224.2:c.158+114_158+115insAGAGC (IDUA) MANE Select ENSP00000425081.2:n.158+114_158+115insAGAGC
ENST00000247933.8:c.158+114_158+115insAGAGC (IDUA) ENSP00000247933.4:n.158+114_158+115insAGAGC
ENST00000398520.6:c.576+3771_576+3772insGCTCT (SLC26A1) ENSP00000381532.2:n.576+3771_576+3772insGCTCT
ENST00000502910.5:c.158+114_158+115insAGAGC (IDUA) ENSP00000422952.1:n.158+114_158+115insAGAGC
ENST00000504568.5:c.156+114_156+115insAGAGC (IDUA)
ENST00000506561.5:n.167+114_167+115insAGAGC (IDUA)
ENST00000508168.5:n.177+114_177+115insAGAGC (IDUA)
ENST00000514698.5:n.199+114_199+115insAGAGC (IDUA)
ENST00000622731.4:c.576+3771_576+3772insGCTCT (SLC26A1) ENSP00000483506.1:n.576+3771_576+3772insGCTCT
NM_000203.4:c.158+114_158+115insAGAGC (IDUA) NP_000194.2:n.158+114_158+115insAGAGC
NM_134425.2:c.576+3771_576+3772insGCTCT (SLC26A1) NP_602297.1:n.576+3771_576+3772insGCTCT
NR_110313.1:n.246+114_246+115insAGAGC (IDUA)
XM_011513459.1:c.158+114_158+115insAGAGC (IDUA) XP_011511761.1:n.158+114_158+115insAGAGC
XM_011513460.1:c.158+114_158+115insAGAGC (IDUA) XP_011511762.1:n.158+114_158+115insAGAGC
XR_924947.1:n.227+114_227+115insAGAGC (IDUA)
NM_000203.5:c.158+114_158+115insAGAGC (IDUA) MANE Select NP_000194.2:n.158+114_158+115insAGAGC
XM_017008163.1:c.-1309+114_-1309+115insAGAGC (IDUA) XP_016863652.1:n.-1309+114_-1309+115insAGAGC
NM_134425.3:c.576+3771_576+3772insGCTCT (SLC26A1) NP_602297.1:n.576+3771_576+3772insGCTCT
NM_134425.4:c.576+3771_576+3772insGCTCT (SLC26A1) NP_602297.1:n.576+3771_576+3772insGCTCT