Canonical Allele Identifier: CA2802158

Gene: IDUA

Linked Data

• dbSNP Id: rs776395091
• ExAC: 4:996075 A / G
• gnomAD v2: 4-996075-A-G
• gnomAD v4: 4-1002287-A-G
• MyVariant Identifiers: chr4:g.996075A>G (hg19) ; chr4:g.1002287A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002287A>G , CM000666.2:g.1002287A>G	GRCh38
NC_000004.11:g.996075A>G , CM000666.1:g.996075A>G	GRCh37
NC_000004.10:g.986075A>G	NCBI36
NG_008103.1:g.20291A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.991A>G	ENSP00000247933.4:p.Asn331Asp
ENST00000514224.2:c.991A>G MANE Select	ENSP00000425081.2:p.Asn331Asp
ENST00000652070.1:n.1047A>G
ENST00000247933.8:c.991A>G	ENSP00000247933.4:p.Asn331Asp
ENST00000514224.1:c.595A>G	ENSP00000425081.1:p.Asn199Asp
ENST00000514698.5:n.1098A>G
NM_000203.4:c.991A>G	NP_000194.2:p.Asn331Asp
NR_110313.1:n.1079A>G
XM_006713882.2:c.595A>G	XP_006713945.1:p.Asn199Asp
XM_011513459.1:c.1057A>G	XP_011511761.1:p.Asn353Asp
XM_011513460.1:c.850A>G	XP_011511762.1:p.Asn284Asp
XM_011513461.1:c.784A>G	XP_011511763.1:p.Asn262Asp
XM_011513462.1:c.703A>G	XP_011511764.1:p.Asn235Asp
XM_011513463.1:c.703A>G	XP_011511765.1:p.Asn235Asp
XR_924947.1:n.1060A>G
NM_000203.5:c.991A>G MANE Select	NP_000194.2:p.Asn331Asp
NM_001363576.1:c.595A>G	NP_001350505.1:p.Asn199Asp
XM_011513461.2:c.784A>G	XP_011511763.1:p.Asn262Asp
XM_017008163.1:c.31A>G	XP_016863652.1:p.Asn11Asp