Canonical Allele Identifier: CA2739858957
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002215G>A , CM000666.2:g.1002215G>A GRCh38
NC_000004.11:g.996003G>A , CM000666.1:g.996003G>A GRCh37
NC_000004.10:g.986003G>A NCBI36
NG_008103.1:g.20219G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.973-54G>A ENSP00000247933.4:n.973-54G>A
ENST00000514224.2:c.973-54G>A MANE Select ENSP00000425081.2:n.973-54G>A
ENST00000652070.1:n.1029-54G>A
ENST00000247933.8:c.973-54G>A ENSP00000247933.4:n.973-54G>A
ENST00000514224.1:c.577-54G>A ENSP00000425081.1:n.577-54G>A
ENST00000514698.5:n.1026G>A
NM_000203.4:c.973-54G>A NP_000194.2:n.973-54G>A
NR_110313.1:n.1061-54G>A
XM_006713882.2:c.577-54G>A XP_006713945.1:n.577-54G>A
XM_011513459.1:c.985G>A XP_011511761.1:p.Asp329Asn
XM_011513460.1:c.832-54G>A XP_011511762.1:n.832-54G>A
XM_011513461.1:c.766-54G>A XP_011511763.1:n.766-54G>A
XM_011513462.1:c.685-54G>A XP_011511764.1:n.685-54G>A
XM_011513463.1:c.685-54G>A XP_011511765.1:n.685-54G>A
XR_924947.1:n.1042-54G>A
NM_000203.5:c.973-54G>A MANE Select NP_000194.2:n.973-54G>A
NM_001363576.1:c.577-54G>A NP_001350505.1:n.577-54G>A
XM_011513461.2:c.766-54G>A XP_011511763.1:n.766-54G>A
XM_017008163.1:c.13-54G>A XP_016863652.1:n.13-54G>A