Canonical Allele Identifier: CA355962842
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002150A>T , CM000666.2:g.1002150A>T GRCh38
NC_000004.11:g.995938A>T , CM000666.1:g.995938A>T GRCh37
NC_000004.10:g.985938A>T NCBI36
NG_008103.1:g.20154A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.961A>T ENSP00000247933.4:p.Met321Leu
ENST00000514224.2:c.961A>T MANE Select ENSP00000425081.2:p.Met321Leu
ENST00000652070.1:n.1017A>T
ENST00000247933.8:c.961A>T ENSP00000247933.4:p.Met321Leu
ENST00000514224.1:c.565A>T ENSP00000425081.1:p.Met189Leu
ENST00000514698.5:n.961A>T
NM_000203.4:c.961A>T NP_000194.2:p.Met321Leu
NR_110313.1:n.1049A>T
XM_006713882.2:c.565A>T XP_006713945.1:p.Met189Leu
XM_011513459.1:c.920A>T XP_011511761.1:p.His307Leu
XM_011513460.1:c.820A>T XP_011511762.1:p.Met274Leu
XM_011513461.1:c.754A>T XP_011511763.1:p.Met252Leu
XM_011513462.1:c.673A>T XP_011511764.1:p.Met225Leu
XM_011513463.1:c.673A>T XP_011511765.1:p.Met225Leu
XR_924947.1:n.1030A>T
NM_000203.5:c.961A>T MANE Select NP_000194.2:p.Met321Leu
NM_001363576.1:c.565A>T NP_001350505.1:p.Met189Leu
XM_011513461.2:c.754A>T XP_011511763.1:p.Met252Leu
XM_017008163.1:c.1A>T XP_016863652.1:p.Met1Leu