Canonical Allele Identifier: CA355965277

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2451016
• ClinVar RCV Id: RCV003182047
• MyVariant Identifiers: chr4:g.997406G>C (hg19) ; chr4:g.1003618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003618G>C , CM000666.2:g.1003618G>C	GRCh38
NC_000004.11:g.997406G>C , CM000666.1:g.997406G>C	GRCh37
NC_000004.10:g.987406G>C	NCBI36
NG_008103.1:g.21622G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1720G>C	ENSP00000247933.4:p.Gly574Arg
ENST00000514224.2:c.1720G>C MANE Select	ENSP00000425081.2:p.Gly574Arg
ENST00000652070.1:n.1776G>C
ENST00000247933.8:c.1720G>C	ENSP00000247933.4:p.Gly574Arg
ENST00000514224.1:c.1324G>C	ENSP00000425081.1:p.Gly442Arg
ENST00000514417.1:n.112G>C
ENST00000514698.5:n.1827G>C
NM_000203.4:c.1720G>C	NP_000194.2:p.Gly574Arg
NR_110313.1:n.1808G>C
XM_006713882.2:c.1324G>C	XP_006713945.1:p.Gly442Arg
XM_011513459.1:c.1786G>C	XP_011511761.1:p.Gly596Arg
XM_011513460.1:c.1579G>C	XP_011511762.1:p.Gly527Arg
XM_011513461.1:c.1513G>C	XP_011511763.1:p.Gly505Arg
XM_011513462.1:c.1432G>C	XP_011511764.1:p.Gly478Arg
XM_011513463.1:c.1432G>C	XP_011511765.1:p.Gly478Arg
XR_924947.1:n.1976G>C
NM_000203.5:c.1720G>C MANE Select	NP_000194.2:p.Gly574Arg
NM_001363576.1:c.1324G>C	NP_001350505.1:p.Gly442Arg
XM_011513461.2:c.1513G>C	XP_011511763.1:p.Gly505Arg
XM_017008163.1:c.760G>C	XP_016863652.1:p.Gly254Arg