Canonical Allele Identifier: CA355963348
Community Standard Title: NM_000203.5(IDUA):c.1108C>T (p.Gln370Ter)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002404C>T , CM000666.2:g.1002404C>T GRCh38
NC_000004.11:g.996192C>T , CM000666.1:g.996192C>T GRCh37
NC_000004.10:g.986192C>T NCBI36
NG_008103.1:g.20408C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.1108C>T MANE Select NP_000194.2:p.Gln370Ter
ENST00000514224.2:c.1108C>T MANE Select ENSP00000425081.2:p.Gln370Ter
NM_000203.4:c.1108C>T NP_000194.2:p.Gln370Ter
NM_001363576.1:c.712C>T NP_001350505.1:p.Gln238Ter
NR_110313.1:n.1196C>T
ENST00000247933.8:c.1108C>T ENSP00000247933.4:p.Gln370Ter
ENST00000247933.9:c.1108C>T ENSP00000247933.4:p.Gln370Ter
ENST00000514224.1:c.712C>T ENSP00000425081.1:p.Gln238Ter
ENST00000514698.5:n.1215C>T
ENST00000652070.1:n.1164C>T
XM_006713882.2:c.712C>T XP_006713945.1:p.Gln238Ter
XM_011513459.1:c.1174C>T XP_011511761.1:p.Gln392Ter
XM_011513460.1:c.967C>T XP_011511762.1:p.Gln323Ter
XM_011513461.1:c.901C>T XP_011511763.1:p.Gln301Ter
XM_011513461.2:c.901C>T XP_011511763.1:p.Gln301Ter
XM_011513462.1:c.820C>T XP_011511764.1:p.Gln274Ter
XM_011513463.1:c.820C>T XP_011511765.1:p.Gln274Ter
XM_017008163.1:c.148C>T XP_016863652.1:p.Gln50Ter
XR_924947.1:n.1177C>T