Canonical Allele Identifier: CA355965242

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997390G>A (hg19) ; chr4:g.1003602G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003602G>A , CM000666.2:g.1003602G>A	GRCh38
NC_000004.11:g.997390G>A , CM000666.1:g.997390G>A	GRCh37
NC_000004.10:g.987390G>A	NCBI36
NG_008103.1:g.21606G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1704G>A	ENSP00000247933.4:p.Trp568Ter
ENST00000514224.2:c.1704G>A MANE Select	ENSP00000425081.2:p.Trp568Ter
ENST00000652070.1:n.1760G>A
ENST00000247933.8:c.1704G>A	ENSP00000247933.4:p.Trp568Ter
ENST00000514224.1:c.1308G>A	ENSP00000425081.1:p.Trp436Ter
ENST00000514417.1:n.96G>A
ENST00000514698.5:n.1811G>A
NM_000203.4:c.1704G>A	NP_000194.2:p.Trp568Ter
NR_110313.1:n.1792G>A
XM_006713882.2:c.1308G>A	XP_006713945.1:p.Trp436Ter
XM_011513459.1:c.1770G>A	XP_011511761.1:p.Trp590Ter
XM_011513460.1:c.1563G>A	XP_011511762.1:p.Trp521Ter
XM_011513461.1:c.1497G>A	XP_011511763.1:p.Trp499Ter
XM_011513462.1:c.1416G>A	XP_011511764.1:p.Trp472Ter
XM_011513463.1:c.1416G>A	XP_011511765.1:p.Trp472Ter
XR_924947.1:n.1960G>A
NM_000203.5:c.1704G>A MANE Select	NP_000194.2:p.Trp568Ter
NM_001363576.1:c.1308G>A	NP_001350505.1:p.Trp436Ter
XM_011513461.2:c.1497G>A	XP_011511763.1:p.Trp499Ter
XM_017008163.1:c.744G>A	XP_016863652.1:p.Trp248Ter