Canonical Allele Identifier: CA355962361

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002017-G-T
• MyVariant Identifiers: chr4:g.995805G>T (hg19) ; chr4:g.1002017G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002017G>T , CM000666.2:g.1002017G>T	GRCh38
NC_000004.11:g.995805G>T , CM000666.1:g.995805G>T	GRCh37
NC_000004.10:g.985805G>T	NCBI36
NG_008103.1:g.20021G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.828G>T	ENSP00000247933.4:p.Glu276Asp
ENST00000514224.2:c.828G>T MANE Select	ENSP00000425081.2:p.Glu276Asp
ENST00000652070.1:n.884G>T
ENST00000247933.8:c.828G>T	ENSP00000247933.4:p.Glu276Asp
ENST00000514192.5:c.645G>T	ENSP00000423685.1:p.Glu215Asp
ENST00000514224.1:c.432G>T	ENSP00000425081.1:p.Glu144Asp
ENST00000514698.5:n.828G>T
NM_000203.4:c.828G>T	NP_000194.2:p.Glu276Asp
NR_110313.1:n.916G>T
XM_006713882.2:c.432G>T	XP_006713945.1:p.Glu144Asp
XM_011513459.1:c.787G>T	XP_011511761.1:p.Glu263Ter
XM_011513460.1:c.687G>T	XP_011511762.1:p.Glu229Asp
XM_011513461.1:c.621G>T	XP_011511763.1:p.Glu207Asp
XM_011513462.1:c.540G>T	XP_011511764.1:p.Glu180Asp
XM_011513463.1:c.540G>T	XP_011511765.1:p.Glu180Asp
XR_924947.1:n.897G>T
NM_000203.5:c.828G>T MANE Select	NP_000194.2:p.Glu276Asp
NM_001363576.1:c.432G>T	NP_001350505.1:p.Glu144Asp
XM_011513461.2:c.621G>T	XP_011511763.1:p.Glu207Asp
XM_017008163.1:c.-133G>T	XP_016863652.1:n.-133G>T