Canonical Allele Identifier: CA355962262

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995662A>T (hg19) ; chr4:g.1001874A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001874A>T , CM000666.2:g.1001874A>T	GRCh38
NC_000004.11:g.995662A>T , CM000666.1:g.995662A>T	GRCh37
NC_000004.10:g.985662A>T	NCBI36
NG_008103.1:g.19878A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.785A>T	ENSP00000247933.4:p.His262Leu
ENST00000514224.2:c.785A>T MANE Select	ENSP00000425081.2:p.His262Leu
ENST00000652070.1:n.841A>T
ENST00000247933.8:c.785A>T	ENSP00000247933.4:p.His262Leu
ENST00000502910.5:c.644A>T	ENSP00000422952.1:p.His215Leu
ENST00000514192.5:c.602A>T	ENSP00000423685.1:p.His201Leu
ENST00000514224.1:c.389A>T	ENSP00000425081.1:p.His130Leu
ENST00000514698.5:n.685A>T
NM_000203.4:c.785A>T	NP_000194.2:p.His262Leu
NR_110313.1:n.873A>T
XM_006713882.2:c.389A>T	XP_006713945.1:p.His130Leu
XM_011513459.1:c.644A>T	XP_011511761.1:p.His215Leu
XM_011513460.1:c.644A>T	XP_011511762.1:p.His215Leu
XM_011513461.1:c.578A>T	XP_011511763.1:p.His193Leu
XM_011513462.1:c.497A>T	XP_011511764.1:p.His166Leu
XM_011513463.1:c.497A>T	XP_011511765.1:p.His166Leu
XR_924947.1:n.854A>T
NM_000203.5:c.785A>T MANE Select	NP_000194.2:p.His262Leu
NM_001363576.1:c.389A>T	NP_001350505.1:p.His130Leu
XM_011513461.2:c.578A>T	XP_011511763.1:p.His193Leu
XM_017008163.1:c.-176A>T	XP_016863652.1:n.-176A>T