Canonical Allele Identifier: CA1433071459

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003186C= , CM000666.2:g.1003186C=	GRCh38
NC_000004.11:g.996974C= , CM000666.1:g.996974C=	GRCh37
NC_000004.10:g.986974C=	NCBI36
NG_008103.1:g.21190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1524+29C=	ENSP00000247933.4:n.1524+29C=
ENST00000514224.2:c.1524+29C= MANE Select	ENSP00000425081.2:n.1524+29C=
ENST00000652070.1:n.1580+29C=
ENST00000247933.8:c.1524+29C=	ENSP00000247933.4:n.1524+29C=
ENST00000502829.1:n.355C=
ENST00000514224.1:c.1128+29C=	ENSP00000425081.1:n.1128+29C=
ENST00000514698.5:n.1631+29C=
NM_000203.4:c.1524+29C=	NP_000194.2:n.1524+29C=
NR_110313.1:n.1612+29C=
XM_006713882.2:c.1128+29C=	XP_006713945.1:n.1128+29C=
XM_011513459.1:c.1590+29C=	XP_011511761.1:n.1590+29C=
XM_011513460.1:c.1383+29C=	XP_011511762.1:n.1383+29C=
XM_011513461.1:c.1317+29C=	XP_011511763.1:n.1317+29C=
XM_011513462.1:c.1236+29C=	XP_011511764.1:n.1236+29C=
XM_011513463.1:c.1236+29C=	XP_011511765.1:n.1236+29C=
XR_924947.1:n.1622C=
NM_000203.5:c.1524+29C= MANE Select	NP_000194.2:n.1524+29C=
NM_001363576.1:c.1128+29C=	NP_001350505.1:n.1128+29C=
XM_011513461.2:c.1317+29C=	XP_011511763.1:n.1317+29C=
XM_017008163.1:c.564+29C=	XP_016863652.1:n.564+29C=