Canonical Allele Identifier: CA355962745

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995921A>G (hg19) ; chr4:g.1002133A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002133A>G , CM000666.2:g.1002133A>G	GRCh38
NC_000004.11:g.995921A>G , CM000666.1:g.995921A>G	GRCh37
NC_000004.10:g.985921A>G	NCBI36
NG_008103.1:g.20137A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.944A>G	ENSP00000247933.4:p.Asp315Gly
ENST00000514224.2:c.944A>G MANE Select	ENSP00000425081.2:p.Asp315Gly
ENST00000652070.1:n.1000A>G
ENST00000247933.8:c.944A>G	ENSP00000247933.4:p.Asp315Gly
ENST00000514224.1:c.548A>G	ENSP00000425081.1:p.Asp183Gly
ENST00000514698.5:n.944A>G
NM_000203.4:c.944A>G	NP_000194.2:p.Asp315Gly
NR_110313.1:n.1032A>G
XM_006713882.2:c.548A>G	XP_006713945.1:p.Asp183Gly
XM_011513459.1:c.903A>G	XP_011511761.1:p.Gly301=
XM_011513460.1:c.803A>G	XP_011511762.1:p.Asp268Gly
XM_011513461.1:c.737A>G	XP_011511763.1:p.Asp246Gly
XM_011513462.1:c.656A>G	XP_011511764.1:p.Asp219Gly
XM_011513463.1:c.656A>G	XP_011511765.1:p.Asp219Gly
XR_924947.1:n.1013A>G
NM_000203.5:c.944A>G MANE Select	NP_000194.2:p.Asp315Gly
NM_001363576.1:c.548A>G	NP_001350505.1:p.Asp183Gly
XM_011513461.2:c.737A>G	XP_011511763.1:p.Asp246Gly
XM_017008163.1:c.-17A>G	XP_016863652.1:n.-17A>G