Canonical Allele Identifier: CA2802018

Gene: IDUA

Linked Data

• dbSNP Id: rs201029971
• ExAC: 4:995434 G / T
• gnomAD v2: 4-995434-G-T
• gnomAD v4: 4-1001646-G-T
• MyVariant Identifiers: chr4:g.995434G>T (hg19) ; chr4:g.1001646G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001646G>T , CM000666.2:g.1001646G>T	GRCh38
NC_000004.11:g.995434G>T , CM000666.1:g.995434G>T	GRCh37
NC_000004.10:g.985434G>T	NCBI36
NG_008103.1:g.19650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.590-33G>T	ENSP00000247933.4:n.590-33G>T
ENST00000514224.2:c.590-33G>T MANE Select	ENSP00000425081.2:n.590-33G>T
ENST00000652070.1:n.646-33G>T
ENST00000247933.8:c.590-33G>T	ENSP00000247933.4:n.590-33G>T
ENST00000502910.5:c.449-33G>T	ENSP00000422952.1:n.449-33G>T
ENST00000504568.5:c.550-33G>T
ENST00000509948.5:c.383-33G>T	ENSP00000424227.1:n.383-33G>T
ENST00000514192.5:c.407-33G>T	ENSP00000423685.1:n.407-33G>T
ENST00000514224.1:c.194-33G>T	ENSP00000425081.1:n.194-33G>T
ENST00000514698.5:n.490-33G>T
NM_000203.4:c.590-33G>T	NP_000194.2:n.590-33G>T
NR_110313.1:n.678-33G>T
XM_006713882.2:c.194-33G>T	XP_006713945.1:n.194-33G>T
XM_011513459.1:c.449-33G>T	XP_011511761.1:n.449-33G>T
XM_011513460.1:c.449-33G>T	XP_011511762.1:n.449-33G>T
XM_011513461.1:c.383-33G>T	XP_011511763.1:n.383-33G>T
XM_011513462.1:c.302-33G>T	XP_011511764.1:n.302-33G>T
XM_011513463.1:c.302-33G>T	XP_011511765.1:n.302-33G>T
XR_924947.1:n.659-33G>T
NM_000203.5:c.590-33G>T MANE Select	NP_000194.2:n.590-33G>T
NM_001363576.1:c.194-33G>T	NP_001350505.1:n.194-33G>T
XM_011513461.2:c.383-33G>T	XP_011511763.1:n.383-33G>T
XM_017008163.1:c.-399-5G>T	XP_016863652.1:n.-399-5G>T