Canonical Allele Identifier: CA2586965967

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2734639
• ClinVar RCV Id: RCV003593300

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002731del , CM000666.2:g.1002731del	GRCh38
NC_000004.11:g.996519del , CM000666.1:g.996519del	GRCh37
NC_000004.10:g.986519del	NCBI36
NG_008103.1:g.20735del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1190-1del	ENSP00000247933.4:n.1190-1del
ENST00000514224.2:c.1190-1del MANE Select	ENSP00000425081.2:n.1190-1del
ENST00000652070.1:n.1246-1del
ENST00000247933.8:c.1190-1del	ENSP00000247933.4:n.1190-1del
ENST00000514224.1:c.794-1del	ENSP00000425081.1:n.794-1del
ENST00000514698.5:n.1297-1del
NM_000203.4:c.1190-1del	NP_000194.2:n.1190-1del
NR_110313.1:n.1278-1del
XM_006713882.2:c.794-1del	XP_006713945.1:n.794-1del
XM_011513459.1:c.1256-1del	XP_011511761.1:n.1256-1del
XM_011513460.1:c.1049-1del	XP_011511762.1:n.1049-1del
XM_011513461.1:c.983-1del	XP_011511763.1:n.983-1del
XM_011513462.1:c.902-1del	XP_011511764.1:n.902-1del
XM_011513463.1:c.902-1del	XP_011511765.1:n.902-1del
XR_924947.1:n.1259-1del
NM_000203.5:c.1190-1del MANE Select	NP_000194.2:n.1190-1del
NM_001363576.1:c.794-1del	NP_001350505.1:n.794-1del
XM_011513461.2:c.983-1del	XP_011511763.1:n.983-1del
XM_017008163.1:c.230-1del	XP_016863652.1:n.230-1del