Canonical Allele Identifier: CA355962969

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996073A>C (hg19) ; chr4:g.1002285A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002285A>C , CM000666.2:g.1002285A>C	GRCh38
NC_000004.11:g.996073A>C , CM000666.1:g.996073A>C	GRCh37
NC_000004.10:g.986073A>C	NCBI36
NG_008103.1:g.20289A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.989A>C	ENSP00000247933.4:p.Gln330Pro
ENST00000514224.2:c.989A>C MANE Select	ENSP00000425081.2:p.Gln330Pro
ENST00000652070.1:n.1045A>C
ENST00000247933.8:c.989A>C	ENSP00000247933.4:p.Gln330Pro
ENST00000514224.1:c.593A>C	ENSP00000425081.1:p.Gln198Pro
ENST00000514698.5:n.1096A>C
NM_000203.4:c.989A>C	NP_000194.2:p.Gln330Pro
NR_110313.1:n.1077A>C
XM_006713882.2:c.593A>C	XP_006713945.1:p.Gln198Pro
XM_011513459.1:c.1055A>C	XP_011511761.1:p.Gln352Pro
XM_011513460.1:c.848A>C	XP_011511762.1:p.Gln283Pro
XM_011513461.1:c.782A>C	XP_011511763.1:p.Gln261Pro
XM_011513462.1:c.701A>C	XP_011511764.1:p.Gln234Pro
XM_011513463.1:c.701A>C	XP_011511765.1:p.Gln234Pro
XR_924947.1:n.1058A>C
NM_000203.5:c.989A>C MANE Select	NP_000194.2:p.Gln330Pro
NM_001363576.1:c.593A>C	NP_001350505.1:p.Gln198Pro
XM_011513461.2:c.782A>C	XP_011511763.1:p.Gln261Pro
XM_017008163.1:c.29A>C	XP_016863652.1:p.Gln10Pro