Canonical Allele Identifier: CA355962944

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996066C>G (hg19) ; chr4:g.1002278C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002278C>G , CM000666.2:g.1002278C>G	GRCh38
NC_000004.11:g.996066C>G , CM000666.1:g.996066C>G	GRCh37
NC_000004.10:g.986066C>G	NCBI36
NG_008103.1:g.20282C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.982C>G	ENSP00000247933.4:p.Gln328Glu
ENST00000514224.2:c.982C>G MANE Select	ENSP00000425081.2:p.Gln328Glu
ENST00000652070.1:n.1038C>G
ENST00000247933.8:c.982C>G	ENSP00000247933.4:p.Gln328Glu
ENST00000514224.1:c.586C>G	ENSP00000425081.1:p.Gln196Glu
ENST00000514698.5:n.1089C>G
NM_000203.4:c.982C>G	NP_000194.2:p.Gln328Glu
NR_110313.1:n.1070C>G
XM_006713882.2:c.586C>G	XP_006713945.1:p.Gln196Glu
XM_011513459.1:c.1048C>G	XP_011511761.1:p.Gln350Glu
XM_011513460.1:c.841C>G	XP_011511762.1:p.Gln281Glu
XM_011513461.1:c.775C>G	XP_011511763.1:p.Gln259Glu
XM_011513462.1:c.694C>G	XP_011511764.1:p.Gln232Glu
XM_011513463.1:c.694C>G	XP_011511765.1:p.Gln232Glu
XR_924947.1:n.1051C>G
NM_000203.5:c.982C>G MANE Select	NP_000194.2:p.Gln328Glu
NM_001363576.1:c.586C>G	NP_001350505.1:p.Gln196Glu
XM_011513461.2:c.775C>G	XP_011511763.1:p.Gln259Glu
XM_017008163.1:c.22C>G	XP_016863652.1:p.Gln8Glu