Canonical Allele Identifier: CA355962143
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001814A>T , CM000666.2:g.1001814A>T GRCh38
NC_000004.11:g.995602A>T , CM000666.1:g.995602A>T GRCh37
NC_000004.10:g.985602A>T NCBI36
NG_008103.1:g.19818A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.725A>T ENSP00000247933.4:p.His242Leu
ENST00000514224.2:c.725A>T MANE Select ENSP00000425081.2:p.His242Leu
ENST00000652070.1:n.781A>T
ENST00000247933.8:c.725A>T ENSP00000247933.4:p.His242Leu
ENST00000502910.5:c.584A>T ENSP00000422952.1:p.His195Leu
ENST00000509948.5:c.518A>T ENSP00000424227.1:p.His173Leu
ENST00000514192.5:c.542A>T ENSP00000423685.1:p.His181Leu
ENST00000514224.1:c.329A>T ENSP00000425081.1:p.His110Leu
ENST00000514698.5:n.625A>T
NM_000203.4:c.725A>T NP_000194.2:p.His242Leu
NR_110313.1:n.813A>T
XM_006713882.2:c.329A>T XP_006713945.1:p.His110Leu
XM_011513459.1:c.584A>T XP_011511761.1:p.His195Leu
XM_011513460.1:c.584A>T XP_011511762.1:p.His195Leu
XM_011513461.1:c.518A>T XP_011511763.1:p.His173Leu
XM_011513462.1:c.437A>T XP_011511764.1:p.His146Leu
XM_011513463.1:c.437A>T XP_011511765.1:p.His146Leu
XR_924947.1:n.794A>T
NM_000203.5:c.725A>T MANE Select NP_000194.2:p.His242Leu
NM_001363576.1:c.329A>T NP_001350505.1:p.His110Leu
XM_011513461.2:c.518A>T XP_011511763.1:p.His173Leu
XM_017008163.1:c.-236A>T XP_016863652.1:n.-236A>T