Canonical Allele Identifier: CA2669475705
Gene: IDUA HGNC NCBI
SLC26A1 HGNC NCBI

Linked Data

gnomAD v4: 4-987381-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.987381T>G , CM000666.2:g.987381T>G GRCh38
NC_000004.11:g.981169T>G , CM000666.1:g.981169T>G GRCh37
NC_000004.10:g.971169T>G NCBI36
NG_008103.1:g.5385T>G
NG_033042.1:g.11056A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.158+139T>G (IDUA) ENSP00000247933.4:n.158+139T>G
ENST00000514224.2:c.158+139T>G (IDUA) MANE Select ENSP00000425081.2:n.158+139T>G
ENST00000247933.8:c.158+139T>G (IDUA) ENSP00000247933.4:n.158+139T>G
ENST00000398520.6:c.576+3747A>C (SLC26A1) ENSP00000381532.2:n.576+3747A>C
ENST00000502910.5:c.158+139T>G (IDUA) ENSP00000422952.1:n.158+139T>G
ENST00000504568.5:c.156+139T>G (IDUA)
ENST00000506561.5:n.167+139T>G (IDUA)
ENST00000508168.5:n.177+139T>G (IDUA)
ENST00000514698.5:n.199+139T>G (IDUA)
ENST00000622731.4:c.576+3747A>C (SLC26A1) ENSP00000483506.1:n.576+3747A>C
NM_000203.4:c.158+139T>G (IDUA) NP_000194.2:n.158+139T>G
NM_134425.2:c.576+3747A>C (SLC26A1) NP_602297.1:n.576+3747A>C
NR_110313.1:n.246+139T>G (IDUA)
XM_011513459.1:c.158+139T>G (IDUA) XP_011511761.1:n.158+139T>G
XM_011513460.1:c.158+139T>G (IDUA) XP_011511762.1:n.158+139T>G
XR_924947.1:n.227+139T>G (IDUA)
NM_000203.5:c.158+139T>G (IDUA) MANE Select NP_000194.2:n.158+139T>G
XM_017008163.1:c.-1309+139T>G (IDUA) XP_016863652.1:n.-1309+139T>G
NM_134425.3:c.576+3747A>C (SLC26A1) NP_602297.1:n.576+3747A>C
NM_134425.4:c.576+3747A>C (SLC26A1) NP_602297.1:n.576+3747A>C