Canonical Allele Identifier: CA355962737

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995920G>C (hg19) ; chr4:g.1002132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002132G>C , CM000666.2:g.1002132G>C	GRCh38
NC_000004.11:g.995920G>C , CM000666.1:g.995920G>C	GRCh37
NC_000004.10:g.985920G>C	NCBI36
NG_008103.1:g.20136G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.943G>C	ENSP00000247933.4:p.Asp315His
ENST00000514224.2:c.943G>C MANE Select	ENSP00000425081.2:p.Asp315His
ENST00000652070.1:n.999G>C
ENST00000247933.8:c.943G>C	ENSP00000247933.4:p.Asp315His
ENST00000514224.1:c.547G>C	ENSP00000425081.1:p.Asp183His
ENST00000514698.5:n.943G>C
NM_000203.4:c.943G>C	NP_000194.2:p.Asp315His
NR_110313.1:n.1031G>C
XM_006713882.2:c.547G>C	XP_006713945.1:p.Asp183His
XM_011513459.1:c.902G>C	XP_011511761.1:p.Gly301Ala
XM_011513460.1:c.802G>C	XP_011511762.1:p.Asp268His
XM_011513461.1:c.736G>C	XP_011511763.1:p.Asp246His
XM_011513462.1:c.655G>C	XP_011511764.1:p.Asp219His
XM_011513463.1:c.655G>C	XP_011511765.1:p.Asp219His
XR_924947.1:n.1012G>C
NM_000203.5:c.943G>C MANE Select	NP_000194.2:p.Asp315His
NM_001363576.1:c.547G>C	NP_001350505.1:p.Asp183His
XM_011513461.2:c.736G>C	XP_011511763.1:p.Asp246His
XM_017008163.1:c.-18G>C	XP_016863652.1:n.-18G>C