Canonical Allele Identifier: CA2669479266

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2838782
• ClinVar RCV Id: RCV003755682
• gnomAD v4: 4-1001668-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001668C>A , CM000666.2:g.1001668C>A	GRCh38
NC_000004.11:g.995456C>A , CM000666.1:g.995456C>A	GRCh37
NC_000004.10:g.985456C>A	NCBI36
NG_008103.1:g.19672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.590-11C>A	ENSP00000247933.4:n.590-11C>A
ENST00000514224.2:c.590-11C>A MANE Select	ENSP00000425081.2:n.590-11C>A
ENST00000652070.1:n.646-11C>A
ENST00000247933.8:c.590-11C>A	ENSP00000247933.4:n.590-11C>A
ENST00000502910.5:c.449-11C>A	ENSP00000422952.1:n.449-11C>A
ENST00000504568.5:c.550-11C>A
ENST00000509948.5:c.383-11C>A	ENSP00000424227.1:n.383-11C>A
ENST00000514192.5:c.407-11C>A	ENSP00000423685.1:n.407-11C>A
ENST00000514224.1:c.194-11C>A	ENSP00000425081.1:n.194-11C>A
ENST00000514698.5:n.490-11C>A
NM_000203.4:c.590-11C>A	NP_000194.2:n.590-11C>A
NR_110313.1:n.678-11C>A
XM_006713882.2:c.194-11C>A	XP_006713945.1:n.194-11C>A
XM_011513459.1:c.449-11C>A	XP_011511761.1:n.449-11C>A
XM_011513460.1:c.449-11C>A	XP_011511762.1:n.449-11C>A
XM_011513461.1:c.383-11C>A	XP_011511763.1:n.383-11C>A
XM_011513462.1:c.302-11C>A	XP_011511764.1:n.302-11C>A
XM_011513463.1:c.302-11C>A	XP_011511765.1:n.302-11C>A
XR_924947.1:n.659-11C>A
NM_000203.5:c.590-11C>A MANE Select	NP_000194.2:n.590-11C>A
NM_001363576.1:c.194-11C>A	NP_001350505.1:n.194-11C>A
XM_011513461.2:c.383-11C>A	XP_011511763.1:n.383-11C>A
XM_017008163.1:c.-382C>A	XP_016863652.1:n.-382C>A