Canonical Allele Identifier: CA355965287

Gene: IDUA

Linked Data

• gnomAD v4: 4-1003622-C-G
• MyVariant Identifiers: chr4:g.997410C>G (hg19) ; chr4:g.1003622C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003622C>G , CM000666.2:g.1003622C>G	GRCh38
NC_000004.11:g.997410C>G , CM000666.1:g.997410C>G	GRCh37
NC_000004.10:g.987410C>G	NCBI36
NG_008103.1:g.21626C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1724C>G	ENSP00000247933.4:p.Ser575Cys
ENST00000514224.2:c.1724C>G MANE Select	ENSP00000425081.2:p.Ser575Cys
ENST00000652070.1:n.1780C>G
ENST00000247933.8:c.1724C>G	ENSP00000247933.4:p.Ser575Cys
ENST00000514224.1:c.1328C>G	ENSP00000425081.1:p.Ser443Cys
ENST00000514417.1:n.116C>G
ENST00000514698.5:n.1831C>G
NM_000203.4:c.1724C>G	NP_000194.2:p.Ser575Cys
NR_110313.1:n.1812C>G
XM_006713882.2:c.1328C>G	XP_006713945.1:p.Ser443Cys
XM_011513459.1:c.1790C>G	XP_011511761.1:p.Ser597Cys
XM_011513460.1:c.1583C>G	XP_011511762.1:p.Ser528Cys
XM_011513461.1:c.1517C>G	XP_011511763.1:p.Ser506Cys
XM_011513462.1:c.1436C>G	XP_011511764.1:p.Ser479Cys
XM_011513463.1:c.1436C>G	XP_011511765.1:p.Ser479Cys
XR_924947.1:n.1980C>G
NM_000203.5:c.1724C>G MANE Select	NP_000194.2:p.Ser575Cys
NM_001363576.1:c.1328C>G	NP_001350505.1:p.Ser443Cys
XM_011513461.2:c.1517C>G	XP_011511763.1:p.Ser506Cys
XM_017008163.1:c.764C>G	XP_016863652.1:p.Ser255Cys