Canonical Allele Identifier: CA1433068883
Gene: IDUA HGNC NCBI

Linked Data

dbSNP Id: rs1363182930

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002213G>T , CM000666.2:g.1002213G>T GRCh38
NC_000004.11:g.996001G>T , CM000666.1:g.996001G>T GRCh37
NC_000004.10:g.986001G>T NCBI36
NG_008103.1:g.20217G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.972+52G>T ENSP00000247933.4:n.972+52G>T
ENST00000514224.2:c.972+52G>T MANE Select ENSP00000425081.2:n.972+52G>T
ENST00000652070.1:n.1028+52G>T
ENST00000247933.8:c.972+52G>T ENSP00000247933.4:n.972+52G>T
ENST00000514224.1:c.576+52G>T ENSP00000425081.1:n.576+52G>T
ENST00000514698.5:n.1024G>T
NM_000203.4:c.972+52G>T NP_000194.2:n.972+52G>T
NR_110313.1:n.1060+52G>T
XM_006713882.2:c.576+52G>T XP_006713945.1:n.576+52G>T
XM_011513459.1:c.983G>T XP_011511761.1:p.Arg328Leu
XM_011513460.1:c.831+52G>T XP_011511762.1:n.831+52G>T
XM_011513461.1:c.765+52G>T XP_011511763.1:n.765+52G>T
XM_011513462.1:c.684+52G>T XP_011511764.1:n.684+52G>T
XM_011513463.1:c.684+52G>T XP_011511765.1:n.684+52G>T
XR_924947.1:n.1041+52G>T
NM_000203.5:c.972+52G>T MANE Select NP_000194.2:n.972+52G>T
NM_001363576.1:c.576+52G>T NP_001350505.1:n.576+52G>T
XM_011513461.2:c.765+52G>T XP_011511763.1:n.765+52G>T
XM_017008163.1:c.12+52G>T XP_016863652.1:n.12+52G>T