Canonical Allele Identifier: CA784304442

Gene: IDUA

Linked Data

• dbSNP Id: rs1453037681
• MyVariant Identifiers: chr4:g.996014del (hg19) ; chr4:g.1002226del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002227del , CM000666.2:g.1002227del	GRCh38
NC_000004.11:g.996015del , CM000666.1:g.996015del	GRCh37
NC_000004.10:g.986015del	NCBI36
NG_008103.1:g.20231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.973-42del	ENSP00000247933.4:n.973-42del
ENST00000514224.2:c.973-42del MANE Select	ENSP00000425081.2:n.973-42del
ENST00000652070.1:n.1029-42del
ENST00000247933.8:c.973-42del	ENSP00000247933.4:n.973-42del
ENST00000514224.1:c.577-42del	ENSP00000425081.1:n.577-42del
ENST00000514698.5:n.1038del
NM_000203.4:c.973-42del	NP_000194.2:n.973-42del
NR_110313.1:n.1061-42del
XM_006713882.2:c.577-42del	XP_006713945.1:n.577-42del
XM_011513459.1:c.997del	XP_011511761.1:p.Val333TrpfsTer?
XM_011513460.1:c.832-42del	XP_011511762.1:n.832-42del
XM_011513461.1:c.766-42del	XP_011511763.1:n.766-42del
XM_011513462.1:c.685-42del	XP_011511764.1:n.685-42del
XM_011513463.1:c.685-42del	XP_011511765.1:n.685-42del
XR_924947.1:n.1042-42del
NM_000203.5:c.973-42del MANE Select	NP_000194.2:n.973-42del
NM_001363576.1:c.577-42del	NP_001350505.1:n.577-42del
XM_011513461.2:c.766-42del	XP_011511763.1:n.766-42del
XM_017008163.1:c.13-42del	XP_016863652.1:n.13-42del