Canonical Allele Identifier: CA355962245

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995652A>T (hg19) ; chr4:g.1001864A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001864A>T , CM000666.2:g.1001864A>T	GRCh38
NC_000004.11:g.995652A>T , CM000666.1:g.995652A>T	GRCh37
NC_000004.10:g.985652A>T	NCBI36
NG_008103.1:g.19868A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.775A>T	ENSP00000247933.4:p.Ile259Phe
ENST00000514224.2:c.775A>T MANE Select	ENSP00000425081.2:p.Ile259Phe
ENST00000652070.1:n.831A>T
ENST00000247933.8:c.775A>T	ENSP00000247933.4:p.Ile259Phe
ENST00000502910.5:c.634A>T	ENSP00000422952.1:p.Ile212Phe
ENST00000514192.5:c.592A>T	ENSP00000423685.1:p.Ile198Phe
ENST00000514224.1:c.379A>T	ENSP00000425081.1:p.Ile127Phe
ENST00000514698.5:n.675A>T
NM_000203.4:c.775A>T	NP_000194.2:p.Ile259Phe
NR_110313.1:n.863A>T
XM_006713882.2:c.379A>T	XP_006713945.1:p.Ile127Phe
XM_011513459.1:c.634A>T	XP_011511761.1:p.Ile212Phe
XM_011513460.1:c.634A>T	XP_011511762.1:p.Ile212Phe
XM_011513461.1:c.568A>T	XP_011511763.1:p.Ile190Phe
XM_011513462.1:c.487A>T	XP_011511764.1:p.Ile163Phe
XM_011513463.1:c.487A>T	XP_011511765.1:p.Ile163Phe
XR_924947.1:n.844A>T
NM_000203.5:c.775A>T MANE Select	NP_000194.2:p.Ile259Phe
NM_001363576.1:c.379A>T	NP_001350505.1:p.Ile127Phe
XM_011513461.2:c.568A>T	XP_011511763.1:p.Ile190Phe
XM_017008163.1:c.-186A>T	XP_016863652.1:n.-186A>T