Canonical Allele Identifier: CA355963282

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996165G>T (hg19) ; chr4:g.1002377G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002377G>T , CM000666.2:g.1002377G>T	GRCh38
NC_000004.11:g.996165G>T , CM000666.1:g.996165G>T	GRCh37
NC_000004.10:g.986165G>T	NCBI36
NG_008103.1:g.20381G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.1081G>T	ENSP00000247933.4:p.Ala361Ser
ENST00000514224.2:c.1081G>T MANE Select	ENSP00000425081.2:p.Ala361Ser
ENST00000652070.1:n.1137G>T
ENST00000247933.8:c.1081G>T	ENSP00000247933.4:p.Ala361Ser
ENST00000514224.1:c.685G>T	ENSP00000425081.1:p.Ala229Ser
ENST00000514698.5:n.1188G>T
NM_000203.4:c.1081G>T	NP_000194.2:p.Ala361Ser
NR_110313.1:n.1169G>T
XM_006713882.2:c.685G>T	XP_006713945.1:p.Ala229Ser
XM_011513459.1:c.1147G>T	XP_011511761.1:p.Ala383Ser
XM_011513460.1:c.940G>T	XP_011511762.1:p.Ala314Ser
XM_011513461.1:c.874G>T	XP_011511763.1:p.Ala292Ser
XM_011513462.1:c.793G>T	XP_011511764.1:p.Ala265Ser
XM_011513463.1:c.793G>T	XP_011511765.1:p.Ala265Ser
XR_924947.1:n.1150G>T
NM_000203.5:c.1081G>T MANE Select	NP_000194.2:p.Ala361Ser
NM_001363576.1:c.685G>T	NP_001350505.1:p.Ala229Ser
XM_011513461.2:c.874G>T	XP_011511763.1:p.Ala292Ser
XM_017008163.1:c.121G>T	XP_016863652.1:p.Ala41Ser