Canonical Allele Identifier: CA355965045

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997215T>G (hg19) ; chr4:g.1003427T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003427T>G , CM000666.2:g.1003427T>G	GRCh38
NC_000004.11:g.997215T>G , CM000666.1:g.997215T>G	GRCh37
NC_000004.10:g.987215T>G	NCBI36
NG_008103.1:g.21431T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.1607T>G	ENSP00000247933.4:p.Leu536Trp
ENST00000514224.2:c.1607T>G MANE Select	ENSP00000425081.2:p.Leu536Trp
ENST00000652070.1:n.1663T>G
ENST00000247933.8:c.1607T>G	ENSP00000247933.4:p.Leu536Trp
ENST00000514224.1:c.1211T>G	ENSP00000425081.1:p.Leu404Trp
ENST00000514698.5:n.1714T>G
NM_000203.4:c.1607T>G	NP_000194.2:p.Leu536Trp
NR_110313.1:n.1695T>G
XM_006713882.2:c.1211T>G	XP_006713945.1:p.Leu404Trp
XM_011513459.1:c.1673T>G	XP_011511761.1:p.Leu558Trp
XM_011513460.1:c.1466T>G	XP_011511762.1:p.Leu489Trp
XM_011513461.1:c.1400T>G	XP_011511763.1:p.Leu467Trp
XM_011513462.1:c.1319T>G	XP_011511764.1:p.Leu440Trp
XM_011513463.1:c.1319T>G	XP_011511765.1:p.Leu440Trp
XR_924947.1:n.1863T>G
NM_000203.5:c.1607T>G MANE Select	NP_000194.2:p.Leu536Trp
NM_001363576.1:c.1211T>G	NP_001350505.1:p.Leu404Trp
XM_011513461.2:c.1400T>G	XP_011511763.1:p.Leu467Trp
XM_017008163.1:c.647T>G	XP_016863652.1:p.Leu216Trp