Canonical Allele Identifier: CA1433071748

Gene: IDUA

Linked Data

• ClinVar Variation Id: 1111099
• ClinVar RCV Id: RCV001437541
• dbSNP Id: rs1715234723

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003341C>G , CM000666.2:g.1003341C>G	GRCh38
NC_000004.11:g.997129C>G , CM000666.1:g.997129C>G	GRCh37
NC_000004.10:g.987129C>G	NCBI36
NG_008103.1:g.21345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1525-4C>G	ENSP00000247933.4:n.1525-4C>G
ENST00000514224.2:c.1525-4C>G MANE Select	ENSP00000425081.2:n.1525-4C>G
ENST00000652070.1:n.1581-4C>G
ENST00000247933.8:c.1525-4C>G	ENSP00000247933.4:n.1525-4C>G
ENST00000502829.1:n.510C>G
ENST00000514224.1:c.1129-4C>G	ENSP00000425081.1:n.1129-4C>G
ENST00000514698.5:n.1632-4C>G
NM_000203.4:c.1525-4C>G	NP_000194.2:n.1525-4C>G
NR_110313.1:n.1613-4C>G
XM_006713882.2:c.1129-4C>G	XP_006713945.1:n.1129-4C>G
XM_011513459.1:c.1591-4C>G	XP_011511761.1:n.1591-4C>G
XM_011513460.1:c.1384-4C>G	XP_011511762.1:n.1384-4C>G
XM_011513461.1:c.1318-4C>G	XP_011511763.1:n.1318-4C>G
XM_011513462.1:c.1237-4C>G	XP_011511764.1:n.1237-4C>G
XM_011513463.1:c.1237-4C>G	XP_011511765.1:n.1237-4C>G
XR_924947.1:n.1777C>G
NM_000203.5:c.1525-4C>G MANE Select	NP_000194.2:n.1525-4C>G
NM_001363576.1:c.1129-4C>G	NP_001350505.1:n.1129-4C>G
XM_011513461.2:c.1318-4C>G	XP_011511763.1:n.1318-4C>G
XM_017008163.1:c.565-4C>G	XP_016863652.1:n.565-4C>G