Canonical Allele Identifier: CA355963314

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996174A>T (hg19) ; chr4:g.1002386A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002386A>T , CM000666.2:g.1002386A>T	GRCh38
NC_000004.11:g.996174A>T , CM000666.1:g.996174A>T	GRCh37
NC_000004.10:g.986174A>T	NCBI36
NG_008103.1:g.20390A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.1090A>T	ENSP00000247933.4:p.Thr364Ser
ENST00000514224.2:c.1090A>T MANE Select	ENSP00000425081.2:p.Thr364Ser
ENST00000652070.1:n.1146A>T
ENST00000247933.8:c.1090A>T	ENSP00000247933.4:p.Thr364Ser
ENST00000514224.1:c.694A>T	ENSP00000425081.1:p.Thr232Ser
ENST00000514698.5:n.1197A>T
NM_000203.4:c.1090A>T	NP_000194.2:p.Thr364Ser
NR_110313.1:n.1178A>T
XM_006713882.2:c.694A>T	XP_006713945.1:p.Thr232Ser
XM_011513459.1:c.1156A>T	XP_011511761.1:p.Thr386Ser
XM_011513460.1:c.949A>T	XP_011511762.1:p.Thr317Ser
XM_011513461.1:c.883A>T	XP_011511763.1:p.Thr295Ser
XM_011513462.1:c.802A>T	XP_011511764.1:p.Thr268Ser
XM_011513463.1:c.802A>T	XP_011511765.1:p.Thr268Ser
XR_924947.1:n.1159A>T
NM_000203.5:c.1090A>T MANE Select	NP_000194.2:p.Thr364Ser
NM_001363576.1:c.694A>T	NP_001350505.1:p.Thr232Ser
XM_011513461.2:c.883A>T	XP_011511763.1:p.Thr295Ser
XM_017008163.1:c.130A>T	XP_016863652.1:p.Thr44Ser