Canonical Allele Identifier: CA355962659

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995905C>G (hg19) ; chr4:g.1002117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002117C>G , CM000666.2:g.1002117C>G	GRCh38
NC_000004.11:g.995905C>G , CM000666.1:g.995905C>G	GRCh37
NC_000004.10:g.985905C>G	NCBI36
NG_008103.1:g.20121C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.928C>G	ENSP00000247933.4:p.Gln310Glu
ENST00000514224.2:c.928C>G MANE Select	ENSP00000425081.2:p.Gln310Glu
ENST00000652070.1:n.984C>G
ENST00000247933.8:c.928C>G	ENSP00000247933.4:p.Gln310Glu
ENST00000514224.1:c.532C>G	ENSP00000425081.1:p.Gln178Glu
ENST00000514698.5:n.928C>G
NM_000203.4:c.928C>G	NP_000194.2:p.Gln310Glu
NR_110313.1:n.1016C>G
XM_006713882.2:c.532C>G	XP_006713945.1:p.Gln178Glu
XM_011513459.1:c.887C>G	XP_011511761.1:p.Thr296Arg
XM_011513460.1:c.787C>G	XP_011511762.1:p.Gln263Glu
XM_011513461.1:c.721C>G	XP_011511763.1:p.Gln241Glu
XM_011513462.1:c.640C>G	XP_011511764.1:p.Gln214Glu
XM_011513463.1:c.640C>G	XP_011511765.1:p.Gln214Glu
XR_924947.1:n.997C>G
NM_000203.5:c.928C>G MANE Select	NP_000194.2:p.Gln310Glu
NM_001363576.1:c.532C>G	NP_001350505.1:p.Gln178Glu
XM_011513461.2:c.721C>G	XP_011511763.1:p.Gln241Glu
XM_017008163.1:c.-33C>G	XP_016863652.1:n.-33C>G