Canonical Allele Identifier: CA2669480364

Gene: IDUA

Linked Data

• gnomAD v4: 4-1001969-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001973del , CM000666.2:g.1001973del	GRCh38
NC_000004.11:g.995761del , CM000666.1:g.995761del	GRCh37
NC_000004.10:g.985761del	NCBI36
NG_008103.1:g.19977del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.793-9del	ENSP00000247933.4:n.793-9del
ENST00000514224.2:c.793-9del MANE Select	ENSP00000425081.2:n.793-9del
ENST00000652070.1:n.849-9del
ENST00000247933.8:c.793-9del	ENSP00000247933.4:n.793-9del
ENST00000502910.5:c.652-9del	ENSP00000422952.1:n.652-9del
ENST00000514192.5:c.610-9del	ENSP00000423685.1:n.610-9del
ENST00000514224.1:c.397-9del	ENSP00000425081.1:n.397-9del
ENST00000514698.5:n.784del
NM_000203.4:c.793-9del	NP_000194.2:n.793-9del
NR_110313.1:n.881-9del
XM_006713882.2:c.397-9del	XP_006713945.1:n.397-9del
XM_011513459.1:c.743del	XP_011511761.1:p.Pro248ArgfsTer?
XM_011513460.1:c.652-9del	XP_011511762.1:n.652-9del
XM_011513461.1:c.586-9del	XP_011511763.1:n.586-9del
XM_011513462.1:c.505-9del	XP_011511764.1:n.505-9del
XM_011513463.1:c.505-9del	XP_011511765.1:n.505-9del
XR_924947.1:n.862-9del
NM_000203.5:c.793-9del MANE Select	NP_000194.2:n.793-9del
NM_001363576.1:c.397-9del	NP_001350505.1:n.397-9del
XM_011513461.2:c.586-9del	XP_011511763.1:n.586-9del
XM_017008163.1:c.-168-9del	XP_016863652.1:n.-168-9del