Canonical Allele Identifier: CA355965280

Gene: IDUA

Linked Data

• dbSNP Id: rs1715262165
• MyVariant Identifiers: chr4:g.997407G>A (hg19) ; chr4:g.1003619G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003619G>A , CM000666.2:g.1003619G>A	GRCh38
NC_000004.11:g.997407G>A , CM000666.1:g.997407G>A	GRCh37
NC_000004.10:g.987407G>A	NCBI36
NG_008103.1:g.21623G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1721G>A	ENSP00000247933.4:p.Gly574Asp
ENST00000514224.2:c.1721G>A MANE Select	ENSP00000425081.2:p.Gly574Asp
ENST00000652070.1:n.1777G>A
ENST00000247933.8:c.1721G>A	ENSP00000247933.4:p.Gly574Asp
ENST00000514224.1:c.1325G>A	ENSP00000425081.1:p.Gly442Asp
ENST00000514417.1:n.113G>A
ENST00000514698.5:n.1828G>A
NM_000203.4:c.1721G>A	NP_000194.2:p.Gly574Asp
NR_110313.1:n.1809G>A
XM_006713882.2:c.1325G>A	XP_006713945.1:p.Gly442Asp
XM_011513459.1:c.1787G>A	XP_011511761.1:p.Gly596Asp
XM_011513460.1:c.1580G>A	XP_011511762.1:p.Gly527Asp
XM_011513461.1:c.1514G>A	XP_011511763.1:p.Gly505Asp
XM_011513462.1:c.1433G>A	XP_011511764.1:p.Gly478Asp
XM_011513463.1:c.1433G>A	XP_011511765.1:p.Gly478Asp
XR_924947.1:n.1977G>A
NM_000203.5:c.1721G>A MANE Select	NP_000194.2:p.Gly574Asp
NM_001363576.1:c.1325G>A	NP_001350505.1:p.Gly442Asp
XM_011513461.2:c.1514G>A	XP_011511763.1:p.Gly505Asp
XM_017008163.1:c.761G>A	XP_016863652.1:p.Gly254Asp