Canonical Allele Identifier: CA355963525

Gene: IDUA

Linked Data

• dbSNP Id: rs1715176008
• MyVariant Identifiers: chr4:g.996524G>C (hg19) ; chr4:g.1002736G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002736G>C , CM000666.2:g.1002736G>C	GRCh38
NC_000004.11:g.996524G>C , CM000666.1:g.996524G>C	GRCh37
NC_000004.10:g.986524G>C	NCBI36
NG_008103.1:g.20740G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1194G>C	ENSP00000247933.4:p.Glu398Asp
ENST00000514224.2:c.1194G>C MANE Select	ENSP00000425081.2:p.Glu398Asp
ENST00000652070.1:n.1250G>C
ENST00000247933.8:c.1194G>C	ENSP00000247933.4:p.Glu398Asp
ENST00000514224.1:c.798G>C	ENSP00000425081.1:p.Glu266Asp
ENST00000514698.5:n.1301G>C
NM_000203.4:c.1194G>C	NP_000194.2:p.Glu398Asp
NR_110313.1:n.1282G>C
XM_006713882.2:c.798G>C	XP_006713945.1:p.Glu266Asp
XM_011513459.1:c.1260G>C	XP_011511761.1:p.Glu420Asp
XM_011513460.1:c.1053G>C	XP_011511762.1:p.Glu351Asp
XM_011513461.1:c.987G>C	XP_011511763.1:p.Glu329Asp
XM_011513462.1:c.906G>C	XP_011511764.1:p.Glu302Asp
XM_011513463.1:c.906G>C	XP_011511765.1:p.Glu302Asp
XR_924947.1:n.1263G>C
NM_000203.5:c.1194G>C MANE Select	NP_000194.2:p.Glu398Asp
NM_001363576.1:c.798G>C	NP_001350505.1:p.Glu266Asp
XM_011513461.2:c.987G>C	XP_011511763.1:p.Glu329Asp
XM_017008163.1:c.234G>C	XP_016863652.1:p.Glu78Asp