Canonical Allele Identifier: CA2669482329

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002713-G-GCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002716_1002722dup , CM000666.2:g.1002716_1002722dup	GRCh38
NC_000004.11:g.996504_996510dup , CM000666.1:g.996504_996510dup	GRCh37
NC_000004.10:g.986504_986510dup	NCBI36
NG_008103.1:g.20720_20726dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1190-16_1190-10dup	ENSP00000247933.4:n.1190-16_1190-10dup
ENST00000514224.2:c.1190-16_1190-10dup MANE Select	ENSP00000425081.2:n.1190-16_1190-10dup
ENST00000652070.1:n.1246-16_1246-10dup
ENST00000247933.8:c.1190-16_1190-10dup	ENSP00000247933.4:n.1190-16_1190-10dup
ENST00000514224.1:c.794-16_794-10dup	ENSP00000425081.1:n.794-16_794-10dup
ENST00000514698.5:n.1297-16_1297-10dup
NM_000203.4:c.1190-16_1190-10dup	NP_000194.2:n.1190-16_1190-10dup
NR_110313.1:n.1278-16_1278-10dup
XM_006713882.2:c.794-16_794-10dup	XP_006713945.1:n.794-16_794-10dup
XM_011513459.1:c.1256-16_1256-10dup	XP_011511761.1:n.1256-16_1256-10dup
XM_011513460.1:c.1049-16_1049-10dup	XP_011511762.1:n.1049-16_1049-10dup
XM_011513461.1:c.983-16_983-10dup	XP_011511763.1:n.983-16_983-10dup
XM_011513462.1:c.902-16_902-10dup	XP_011511764.1:n.902-16_902-10dup
XM_011513463.1:c.902-16_902-10dup	XP_011511765.1:n.902-16_902-10dup
XR_924947.1:n.1259-16_1259-10dup
NM_000203.5:c.1190-16_1190-10dup MANE Select	NP_000194.2:n.1190-16_1190-10dup
NM_001363576.1:c.794-16_794-10dup	NP_001350505.1:n.794-16_794-10dup
XM_011513461.2:c.983-16_983-10dup	XP_011511763.1:n.983-16_983-10dup
XM_017008163.1:c.230-16_230-10dup	XP_016863652.1:n.230-16_230-10dup