Canonical Allele Identifier: CA438057987

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2840145
• ClinVar RCV Id: RCV003755696
• gnomAD v4: 4-1003464-C-G
• MyVariant Identifiers: chr4:g.997252C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003464C>G , CM000666.2:g.1003464C>G	GRCh38
NC_000004.11:g.997252C>G , CM000666.1:g.997252C>G	GRCh37
NC_000004.10:g.987252C>G	NCBI36
NG_008103.1:g.21468C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1644C>G	ENSP00000247933.4:p.Pro548=
ENST00000514224.2:c.1644C>G MANE Select	ENSP00000425081.2:p.Pro548=
ENST00000652070.1:n.1700C>G
ENST00000247933.8:c.1644C>G	ENSP00000247933.4:p.Pro548=
ENST00000514224.1:c.1248C>G	ENSP00000425081.1:p.Pro416=
ENST00000514417.1:n.36C>G
ENST00000514698.5:n.1751C>G
NM_000203.4:c.1644C>G	NP_000194.2:p.Pro548=
NR_110313.1:n.1732C>G
XM_006713882.2:c.1248C>G	XP_006713945.1:p.Pro416=
XM_011513459.1:c.1710C>G	XP_011511761.1:p.Pro570=
XM_011513460.1:c.1503C>G	XP_011511762.1:p.Pro501=
XM_011513461.1:c.1437C>G	XP_011511763.1:p.Pro479=
XM_011513462.1:c.1356C>G	XP_011511764.1:p.Pro452=
XM_011513463.1:c.1356C>G	XP_011511765.1:p.Pro452=
XR_924947.1:n.1900C>G
NM_000203.5:c.1644C>G MANE Select	NP_000194.2:p.Pro548=
NM_001363576.1:c.1248C>G	NP_001350505.1:p.Pro416=
XM_011513461.2:c.1437C>G	XP_011511763.1:p.Pro479=
XM_017008163.1:c.684C>G	XP_016863652.1:p.Pro228=