Canonical Allele Identifier: CA2578014036

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001452del , CM000666.2:g.1001452del	GRCh38
NC_000004.11:g.995240del , CM000666.1:g.995240del	GRCh37
NC_000004.10:g.985240del	NCBI36
NG_008103.1:g.19456del

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.494-16del	ENSP00000247933.4:n.494-16del
ENST00000514224.2:c.494-16del MANE Select	ENSP00000425081.2:n.494-16del
ENST00000652070.1:n.550-16del
ENST00000247933.8:c.494-16del	ENSP00000247933.4:n.494-16del
ENST00000502910.5:c.353-16del	ENSP00000422952.1:n.353-16del
ENST00000504568.5:c.454-16del
ENST00000509948.5:c.287-16del	ENSP00000424227.1:n.287-16del
ENST00000514192.5:c.311-16del	ENSP00000423685.1:n.311-16del
ENST00000514224.1:c.98-16del	ENSP00000425081.1:n.98-16del
ENST00000514698.5:n.394-16del
NM_000203.4:c.494-16del	NP_000194.2:n.494-16del
NR_110313.1:n.582-16del
XM_006713882.2:c.98-16del	XP_006713945.1:n.98-16del
XM_011513459.1:c.353-16del	XP_011511761.1:n.353-16del
XM_011513460.1:c.353-16del	XP_011511762.1:n.353-16del
XM_011513461.1:c.287-16del	XP_011511763.1:n.287-16del
XM_011513462.1:c.206-16del	XP_011511764.1:n.206-16del
XM_011513463.1:c.206-16del	XP_011511765.1:n.206-16del
XR_924947.1:n.563-16del
NM_000203.5:c.494-16del MANE Select	NP_000194.2:n.494-16del
NM_001363576.1:c.98-16del	NP_001350505.1:n.98-16del
XM_011513461.2:c.287-16del	XP_011511763.1:n.287-16del
XM_017008163.1:c.-511del	XP_016863652.1:n.-511del