Canonical Allele Identifier: CA355965328
Community Standard Title: NM_000203.5(IDUA):c.1737G>A (p.Trp579Ter)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1004021G>A , CM000666.2:g.1004021G>A GRCh38
NC_000004.11:g.997809G>A , CM000666.1:g.997809G>A GRCh37
NC_000004.10:g.987809G>A NCBI36
NG_008103.1:g.22025G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.1737G>A MANE Select NP_000194.2:p.Trp579Ter
ENST00000514224.2:c.1737G>A MANE Select ENSP00000425081.2:p.Trp579Ter
NM_000203.4:c.1737G>A NP_000194.2:p.Trp579Ter
NM_001363576.1:c.1341G>A NP_001350505.1:p.Trp447Ter
NR_110313.1:n.1829G>A
ENST00000247933.8:c.1737G>A ENSP00000247933.4:p.Trp579Ter
ENST00000247933.9:c.1737G>A ENSP00000247933.4:p.Trp579Ter
ENST00000514224.1:c.1341G>A ENSP00000425081.1:p.Trp447Ter
ENST00000514698.5:n.1848G>A
ENST00000652070.1:n.1793G>A
XM_006713882.2:c.1341G>A XP_006713945.1:p.Trp447Ter
XM_011513459.1:c.1803G>A XP_011511761.1:p.Trp601Ter
XM_011513460.1:c.1596G>A XP_011511762.1:p.Trp532Ter
XM_011513461.1:c.1530G>A XP_011511763.1:p.Trp510Ter
XM_011513461.2:c.1530G>A XP_011511763.1:p.Trp510Ter
XM_011513462.1:c.1449G>A XP_011511764.1:p.Trp483Ter
XM_011513463.1:c.1449G>A XP_011511765.1:p.Trp483Ter
XM_017008163.1:c.777G>A XP_016863652.1:p.Trp259Ter
XR_924947.1:n.1997G>A