Canonical Allele Identifier: CA2801966
Community Standard Title: NM_000203.5(IDUA):c.494G>A (p.Gly165Asp)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001468G>A , CM000666.2:g.1001468G>A GRCh38
NC_000004.11:g.995256G>A , CM000666.1:g.995256G>A GRCh37
NC_000004.10:g.985256G>A NCBI36
NG_008103.1:g.19472G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.494G>A MANE Select NP_000194.2:p.Gly165Asp
ENST00000514224.2:c.494G>A MANE Select ENSP00000425081.2:p.Gly165Asp
NM_000203.4:c.494G>A NP_000194.2:p.Gly165Asp
NM_001363576.1:c.98G>A NP_001350505.1:p.Gly33Asp
NR_110313.1:n.582G>A
ENST00000247933.8:c.494G>A ENSP00000247933.4:p.Gly165Asp
ENST00000247933.9:c.494G>A ENSP00000247933.4:p.Gly165Asp
ENST00000502910.5:c.353G>A ENSP00000422952.1:p.Gly118Asp
ENST00000504568.5:c.454G>A
ENST00000509948.5:c.287G>A ENSP00000424227.1:p.Gly96Asp
ENST00000514192.5:c.311G>A ENSP00000423685.1:p.Gly104Asp
ENST00000514224.1:c.98G>A ENSP00000425081.1:p.Gly33Asp
ENST00000514698.5:n.394G>A
ENST00000652070.1:n.550G>A
XM_006713882.2:c.98G>A XP_006713945.1:p.Gly33Asp
XM_011513459.1:c.353G>A XP_011511761.1:p.Gly118Asp
XM_011513460.1:c.353G>A XP_011511762.1:p.Gly118Asp
XM_011513461.1:c.287G>A XP_011511763.1:p.Gly96Asp
XM_011513461.2:c.287G>A XP_011511763.1:p.Gly96Asp
XM_011513462.1:c.206G>A XP_011511764.1:p.Gly69Asp
XM_011513463.1:c.206G>A XP_011511765.1:p.Gly69Asp
XM_017008163.1:c.-495G>A XP_016863652.1:n.-495G>A
XR_924947.1:n.563G>A