Canonical Allele Identifier: CA2802248

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003030C>G , CM000666.2:g.1003030C>G	GRCh38
NC_000004.11:g.996818C>G , CM000666.1:g.996818C>G	GRCh37
NC_000004.10:g.986818C>G	NCBI36
NG_008103.1:g.21034C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.1403-6C>G MANE Select	NP_000194.2:n.1403-6C>G
ENST00000514224.2:c.1403-6C>G MANE Select	ENSP00000425081.2:n.1403-6C>G
NM_000203.4:c.1403-6C>G	NP_000194.2:n.1403-6C>G
NM_001363576.1:c.1007-6C>G	NP_001350505.1:n.1007-6C>G
NR_110313.1:n.1491-6C>G
ENST00000247933.8:c.1403-6C>G	ENSP00000247933.4:n.1403-6C>G
ENST00000247933.9:c.1403-6C>G	ENSP00000247933.4:n.1403-6C>G
ENST00000502829.1:n.205-6C>G
ENST00000514224.1:c.1007-6C>G	ENSP00000425081.1:n.1007-6C>G
ENST00000514698.5:n.1510-6C>G
ENST00000652070.1:n.1459-6C>G
XM_006713882.2:c.1007-6C>G	XP_006713945.1:n.1007-6C>G
XM_011513459.1:c.1469-6C>G	XP_011511761.1:n.1469-6C>G
XM_011513460.1:c.1262-6C>G	XP_011511762.1:n.1262-6C>G
XM_011513461.1:c.1196-6C>G	XP_011511763.1:n.1196-6C>G
XM_011513461.2:c.1196-6C>G	XP_011511763.1:n.1196-6C>G
XM_011513462.1:c.1115-6C>G	XP_011511764.1:n.1115-6C>G
XM_011513463.1:c.1115-6C>G	XP_011511765.1:n.1115-6C>G
XM_017008163.1:c.443-6C>G	XP_016863652.1:n.443-6C>G
XR_924947.1:n.1472-6C>G