Canonical Allele Identifier: CA438058015

Gene: IDUA

Linked Data

• ClinVar Variation Id: 2654541
• ClinVar RCV Id: RCV003434917 ; RCV003755038
• gnomAD v4: 4-1003142-C-T
• MyVariant Identifiers: chr4:g.996930C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003142C>T , CM000666.2:g.1003142C>T	GRCh38
NC_000004.11:g.996930C>T , CM000666.1:g.996930C>T	GRCh37
NC_000004.10:g.986930C>T	NCBI36
NG_008103.1:g.21146C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1509C>T	ENSP00000247933.4:p.Arg503=
ENST00000514224.2:c.1509C>T MANE Select	ENSP00000425081.2:p.Arg503=
ENST00000652070.1:n.1565C>T
ENST00000247933.8:c.1509C>T	ENSP00000247933.4:p.Arg503=
ENST00000502829.1:n.311C>T
ENST00000514224.1:c.1113C>T	ENSP00000425081.1:p.Arg371=
ENST00000514698.5:n.1616C>T
NM_000203.4:c.1509C>T	NP_000194.2:p.Arg503=
NR_110313.1:n.1597C>T
XM_006713882.2:c.1113C>T	XP_006713945.1:p.Arg371=
XM_011513459.1:c.1575C>T	XP_011511761.1:p.Arg525=
XM_011513460.1:c.1368C>T	XP_011511762.1:p.Arg456=
XM_011513461.1:c.1302C>T	XP_011511763.1:p.Arg434=
XM_011513462.1:c.1221C>T	XP_011511764.1:p.Arg407=
XM_011513463.1:c.1221C>T	XP_011511765.1:p.Arg407=
XR_924947.1:n.1578C>T
NM_000203.5:c.1509C>T MANE Select	NP_000194.2:p.Arg503=
NM_001363576.1:c.1113C>T	NP_001350505.1:p.Arg371=
XM_011513461.2:c.1302C>T	XP_011511763.1:p.Arg434=
XM_017008163.1:c.549C>T	XP_016863652.1:p.Arg183=