Canonical Allele Identifier: CA1433068716
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002121C= , CM000666.2:g.1002121C= GRCh38
NC_000004.11:g.995909C= , CM000666.1:g.995909C= GRCh37
NC_000004.10:g.985909C= NCBI36
NG_008103.1:g.20125C=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.932C= ENSP00000247933.4:p.Pro311=
ENST00000514224.2:c.932C= MANE Select ENSP00000425081.2:p.Pro311=
ENST00000652070.1:n.988C=
ENST00000247933.8:c.932C= ENSP00000247933.4:p.Pro311=
ENST00000514224.1:c.536C= ENSP00000425081.1:p.Pro179=
ENST00000514698.5:n.932C=
NM_000203.4:c.932C= NP_000194.2:p.Pro311=
NR_110313.1:n.1020C=
XM_006713882.2:c.536C= XP_006713945.1:p.Pro179=
XM_011513459.1:c.891C= XP_011511761.1:p.Ala297=
XM_011513460.1:c.791C= XP_011511762.1:p.Pro264=
XM_011513461.1:c.725C= XP_011511763.1:p.Pro242=
XM_011513462.1:c.644C= XP_011511764.1:p.Pro215=
XM_011513463.1:c.644C= XP_011511765.1:p.Pro215=
XR_924947.1:n.1001C=
NM_000203.5:c.932C= MANE Select NP_000194.2:p.Pro311=
NM_001363576.1:c.536C= NP_001350505.1:p.Pro179=
XM_011513461.2:c.725C= XP_011511763.1:p.Pro242=
XM_017008163.1:c.-29C= XP_016863652.1:n.-29C=