Canonical Allele Identifier: CA355963974
Community Standard Title: NM_000203.5(IDUA):c.1323C>G (p.Tyr441Ter)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002865C>G , CM000666.2:g.1002865C>G GRCh38
NC_000004.11:g.996653C>G , CM000666.1:g.996653C>G GRCh37
NC_000004.10:g.986653C>G NCBI36
NG_008103.1:g.20869C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.1323C>G MANE Select NP_000194.2:p.Tyr441Ter
ENST00000514224.2:c.1323C>G MANE Select ENSP00000425081.2:p.Tyr441Ter
NM_000203.4:c.1323C>G NP_000194.2:p.Tyr441Ter
NM_001363576.1:c.927C>G NP_001350505.1:p.Tyr309Ter
NR_110313.1:n.1411C>G
ENST00000247933.8:c.1323C>G ENSP00000247933.4:p.Tyr441Ter
ENST00000247933.9:c.1323C>G ENSP00000247933.4:p.Tyr441Ter
ENST00000502829.1:n.125C>G
ENST00000514224.1:c.927C>G ENSP00000425081.1:p.Tyr309Ter
ENST00000514698.5:n.1430C>G
ENST00000652070.1:n.1379C>G
XM_006713882.2:c.927C>G XP_006713945.1:p.Tyr309Ter
XM_011513459.1:c.1389C>G XP_011511761.1:p.Tyr463Ter
XM_011513460.1:c.1182C>G XP_011511762.1:p.Tyr394Ter
XM_011513461.1:c.1116C>G XP_011511763.1:p.Tyr372Ter
XM_011513461.2:c.1116C>G XP_011511763.1:p.Tyr372Ter
XM_011513462.1:c.1035C>G XP_011511764.1:p.Tyr345Ter
XM_011513463.1:c.1035C>G XP_011511765.1:p.Tyr345Ter
XM_017008163.1:c.363C>G XP_016863652.1:p.Tyr121Ter
XR_924947.1:n.1392C>G