Canonical Allele Identifier: CA2697557061

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2743591
• ClinVar RCV Id: RCV003591297

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003540del , CM000666.2:g.1003540del	GRCh38
NC_000004.11:g.997328del , CM000666.1:g.997328del	GRCh37
NC_000004.10:g.987328del	NCBI36
NG_008103.1:g.21544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1651-9del	ENSP00000247933.4:n.1651-9del
ENST00000514224.2:c.1651-9del MANE Select	ENSP00000425081.2:n.1651-9del
ENST00000652070.1:n.1707-9del
ENST00000247933.8:c.1651-9del	ENSP00000247933.4:n.1651-9del
ENST00000514224.1:c.1255-9del	ENSP00000425081.1:n.1255-9del
ENST00000514417.1:n.43-9del
ENST00000514698.5:n.1758-9del
NM_000203.4:c.1651-9del	NP_000194.2:n.1651-9del
NR_110313.1:n.1739-9del
XM_006713882.2:c.1255-9del	XP_006713945.1:n.1255-9del
XM_011513459.1:c.1717-9del	XP_011511761.1:n.1717-9del
XM_011513460.1:c.1510-9del	XP_011511762.1:n.1510-9del
XM_011513461.1:c.1444-9del	XP_011511763.1:n.1444-9del
XM_011513462.1:c.1363-9del	XP_011511764.1:n.1363-9del
XM_011513463.1:c.1363-9del	XP_011511765.1:n.1363-9del
XR_924947.1:n.1907-9del
NM_000203.5:c.1651-9del MANE Select	NP_000194.2:n.1651-9del
NM_001363576.1:c.1255-9del	NP_001350505.1:n.1255-9del
XM_011513461.2:c.1444-9del	XP_011511763.1:n.1444-9del
XM_017008163.1:c.691-9del	XP_016863652.1:n.691-9del