Canonical Allele Identifier: CA2669482235
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002711_1002712insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000666.2:g.1002711_1002712insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000004.11:g.996499_996500insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000666.1:g.996499_996500insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000004.10:g.986499_986500insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_008103.1:g.20715_20716insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000247933.4:n.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGG...
ENST00000514224.2:c.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000425081.2:n.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGG...
ENST00000652070.1:n.1246-21_1246-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000247933.8:c.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000247933.4:n.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGG...
ENST00000514224.1:c.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000425081.1:n.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000514698.5:n.1297-21_1297-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000203.4:c.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000194.2:n.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
NR_110313.1:n.1278-21_1278-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
XM_006713882.2:c.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_006713945.1:n.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513459.1:c.1256-21_1256-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511761.1:n.1256-21_1256-20insTGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513460.1:c.1049-21_1049-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511762.1:n.1049-21_1049-20insTGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513461.1:c.983-21_983-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511763.1:n.983-21_983-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513462.1:c.902-21_902-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511764.1:n.902-21_902-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513463.1:c.902-21_902-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511765.1:n.902-21_902-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XR_924947.1:n.1259-21_1259-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000203.5:c.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000194.2:n.1190-21_1190-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001363576.1:c.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001350505.1:n.794-21_794-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011513461.2:c.983-21_983-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011511763.1:n.983-21_983-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_017008163.1:c.230-21_230-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_016863652.1:n.230-21_230-20insTGGGGGGGGGGGGGGGGGGGGGGGGGGG...