Canonical Allele Identifier: CA355962275
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001880A>T , CM000666.2:g.1001880A>T GRCh38
NC_000004.11:g.995668A>T , CM000666.1:g.995668A>T GRCh37
NC_000004.10:g.985668A>T NCBI36
NG_008103.1:g.19884A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.791A>T ENSP00000247933.4:p.Lys264Met
ENST00000514224.2:c.791A>T MANE Select ENSP00000425081.2:p.Lys264Met
ENST00000652070.1:n.847A>T
ENST00000247933.8:c.791A>T ENSP00000247933.4:p.Lys264Met
ENST00000502910.5:c.650A>T ENSP00000422952.1:p.Lys217Met
ENST00000514192.5:c.608A>T ENSP00000423685.1:p.Lys203Met
ENST00000514224.1:c.395A>T ENSP00000425081.1:p.Lys132Met
ENST00000514698.5:n.691A>T
NM_000203.4:c.791A>T NP_000194.2:p.Lys264Met
NR_110313.1:n.879A>T
XM_006713882.2:c.395A>T XP_006713945.1:p.Lys132Met
XM_011513459.1:c.650A>T XP_011511761.1:p.Lys217Met
XM_011513460.1:c.650A>T XP_011511762.1:p.Lys217Met
XM_011513461.1:c.584A>T XP_011511763.1:p.Lys195Met
XM_011513462.1:c.503A>T XP_011511764.1:p.Lys168Met
XM_011513463.1:c.503A>T XP_011511765.1:p.Lys168Met
XR_924947.1:n.860A>T
NM_000203.5:c.791A>T MANE Select NP_000194.2:p.Lys264Met
NM_001363576.1:c.395A>T NP_001350505.1:p.Lys132Met
XM_011513461.2:c.584A>T XP_011511763.1:p.Lys195Met
XM_017008163.1:c.-170A>T XP_016863652.1:n.-170A>T