Canonical Allele Identifier: CA438057358

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996170G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002382G>A , CM000666.2:g.1002382G>A	GRCh38
NC_000004.11:g.996170G>A , CM000666.1:g.996170G>A	GRCh37
NC_000004.10:g.986170G>A	NCBI36
NG_008103.1:g.20386G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.1086G>A	ENSP00000247933.4:p.Gln362=
ENST00000514224.2:c.1086G>A MANE Select	ENSP00000425081.2:p.Gln362=
ENST00000652070.1:n.1142G>A
ENST00000247933.8:c.1086G>A	ENSP00000247933.4:p.Gln362=
ENST00000514224.1:c.690G>A	ENSP00000425081.1:p.Gln230=
ENST00000514698.5:n.1193G>A
NM_000203.4:c.1086G>A	NP_000194.2:p.Gln362=
NR_110313.1:n.1174G>A
XM_006713882.2:c.690G>A	XP_006713945.1:p.Gln230=
XM_011513459.1:c.1152G>A	XP_011511761.1:p.Gln384=
XM_011513460.1:c.945G>A	XP_011511762.1:p.Gln315=
XM_011513461.1:c.879G>A	XP_011511763.1:p.Gln293=
XM_011513462.1:c.798G>A	XP_011511764.1:p.Gln266=
XM_011513463.1:c.798G>A	XP_011511765.1:p.Gln266=
XR_924947.1:n.1155G>A
NM_000203.5:c.1086G>A MANE Select	NP_000194.2:p.Gln362=
NM_001363576.1:c.690G>A	NP_001350505.1:p.Gln230=
XM_011513461.2:c.879G>A	XP_011511763.1:p.Gln293=
XM_017008163.1:c.126G>A	XP_016863652.1:p.Gln42=