Canonical Allele Identifier: CA355961782
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001538T>A , CM000666.2:g.1001538T>A GRCh38
NC_000004.11:g.995326T>A , CM000666.1:g.995326T>A GRCh37
NC_000004.10:g.985326T>A NCBI36
NG_008103.1:g.19542T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.564T>A ENSP00000247933.4:p.Phe188Leu
ENST00000514224.2:c.564T>A MANE Select ENSP00000425081.2:p.Phe188Leu
ENST00000652070.1:n.620T>A
ENST00000247933.8:c.564T>A ENSP00000247933.4:p.Phe188Leu
ENST00000502910.5:c.423T>A ENSP00000422952.1:p.Phe141Leu
ENST00000504568.5:c.524T>A
ENST00000509948.5:c.357T>A ENSP00000424227.1:p.Phe119Leu
ENST00000514192.5:c.381T>A ENSP00000423685.1:p.Phe127Leu
ENST00000514224.1:c.168T>A ENSP00000425081.1:p.Phe56Leu
ENST00000514698.5:n.464T>A
NM_000203.4:c.564T>A NP_000194.2:p.Phe188Leu
NR_110313.1:n.652T>A
XM_006713882.2:c.168T>A XP_006713945.1:p.Phe56Leu
XM_011513459.1:c.423T>A XP_011511761.1:p.Phe141Leu
XM_011513460.1:c.423T>A XP_011511762.1:p.Phe141Leu
XM_011513461.1:c.357T>A XP_011511763.1:p.Phe119Leu
XM_011513462.1:c.276T>A XP_011511764.1:p.Phe92Leu
XM_011513463.1:c.276T>A XP_011511765.1:p.Phe92Leu
XR_924947.1:n.633T>A
NM_000203.5:c.564T>A MANE Select NP_000194.2:p.Phe188Leu
NM_001363576.1:c.168T>A NP_001350505.1:p.Phe56Leu
XM_011513461.2:c.357T>A XP_011511763.1:p.Phe119Leu
XM_017008163.1:c.-425T>A XP_016863652.1:n.-425T>A