Canonical Allele Identifier: CA355962882

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995948A>T (hg19) ; chr4:g.1002160A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002160A>T , CM000666.2:g.1002160A>T	GRCh38
NC_000004.11:g.995948A>T , CM000666.1:g.995948A>T	GRCh37
NC_000004.10:g.985948A>T	NCBI36
NG_008103.1:g.20164A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.971A>T	ENSP00000247933.4:p.Lys324Met
ENST00000514224.2:c.971A>T MANE Select	ENSP00000425081.2:p.Lys324Met
ENST00000652070.1:n.1027A>T
ENST00000247933.8:c.971A>T	ENSP00000247933.4:p.Lys324Met
ENST00000514224.1:c.575A>T	ENSP00000425081.1:p.Lys192Met
ENST00000514698.5:n.971A>T
NM_000203.4:c.971A>T	NP_000194.2:p.Lys324Met
NR_110313.1:n.1059A>T
XM_006713882.2:c.575A>T	XP_006713945.1:p.Lys192Met
XM_011513459.1:c.930A>T	XP_011511761.1:p.Glu310Asp
XM_011513460.1:c.830A>T	XP_011511762.1:p.Lys277Met
XM_011513461.1:c.764A>T	XP_011511763.1:p.Lys255Met
XM_011513462.1:c.683A>T	XP_011511764.1:p.Lys228Met
XM_011513463.1:c.683A>T	XP_011511765.1:p.Lys228Met
XR_924947.1:n.1040A>T
NM_000203.5:c.971A>T MANE Select	NP_000194.2:p.Lys324Met
NM_001363576.1:c.575A>T	NP_001350505.1:p.Lys192Met
XM_011513461.2:c.764A>T	XP_011511763.1:p.Lys255Met
XM_017008163.1:c.11A>T	XP_016863652.1:p.Lys4Met