Canonical Allele Identifier: CA1433067452
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001545G= , CM000666.2:g.1001545G= GRCh38
NC_000004.11:g.995333G= , CM000666.1:g.995333G= GRCh37
NC_000004.10:g.985333G= NCBI36
NG_008103.1:g.19549G=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.571G= ENSP00000247933.4:p.Val191=
ENST00000514224.2:c.571G= MANE Select ENSP00000425081.2:p.Val191=
ENST00000652070.1:n.627G=
ENST00000247933.8:c.571G= ENSP00000247933.4:p.Val191=
ENST00000502910.5:c.430G= ENSP00000422952.1:p.Val144=
ENST00000504568.5:c.531G=
ENST00000509948.5:c.364G= ENSP00000424227.1:p.Val122=
ENST00000514192.5:c.388G= ENSP00000423685.1:p.Val130=
ENST00000514224.1:c.175G= ENSP00000425081.1:p.Val59=
ENST00000514698.5:n.471G=
NM_000203.4:c.571G= NP_000194.2:p.Val191=
NR_110313.1:n.659G=
XM_006713882.2:c.175G= XP_006713945.1:p.Val59=
XM_011513459.1:c.430G= XP_011511761.1:p.Val144=
XM_011513460.1:c.430G= XP_011511762.1:p.Val144=
XM_011513461.1:c.364G= XP_011511763.1:p.Val122=
XM_011513462.1:c.283G= XP_011511764.1:p.Val95=
XM_011513463.1:c.283G= XP_011511765.1:p.Val95=
XR_924947.1:n.640G=
NM_000203.5:c.571G= MANE Select NP_000194.2:p.Val191=
NM_001363576.1:c.175G= NP_001350505.1:p.Val59=
XM_011513461.2:c.364G= XP_011511763.1:p.Val122=
XM_017008163.1:c.-418G= XP_016863652.1:n.-418G=