Canonical Allele Identifier: CA2669475633

Gene: IDUA SLC26A1

Linked Data

• gnomAD v4: 4-987356-GCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987358_987361del , CM000666.2:g.987358_987361del	GRCh38
NC_000004.11:g.981146_981149del , CM000666.1:g.981146_981149del	GRCh37
NC_000004.10:g.971146_971149del	NCBI36
NG_008103.1:g.5362_5365del
NG_033042.1:g.11077_11080del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.158+116_158+119del (IDUA)	ENSP00000247933.4:n.158+116_158+119del
ENST00000514224.2:c.158+116_158+119del (IDUA) MANE Select	ENSP00000425081.2:n.158+116_158+119del
ENST00000247933.8:c.158+116_158+119del (IDUA)	ENSP00000247933.4:n.158+116_158+119del
ENST00000398520.6:c.576+3768_576+3771del (SLC26A1)	ENSP00000381532.2:n.576+3768_576+3771del
ENST00000502910.5:c.158+116_158+119del (IDUA)	ENSP00000422952.1:n.158+116_158+119del
ENST00000504568.5:c.156+116_156+119del (IDUA)
ENST00000506561.5:n.167+116_167+119del (IDUA)
ENST00000508168.5:n.177+116_177+119del (IDUA)
ENST00000514698.5:n.199+116_199+119del (IDUA)
ENST00000622731.4:c.576+3768_576+3771del (SLC26A1)	ENSP00000483506.1:n.576+3768_576+3771del
NM_000203.4:c.158+116_158+119del (IDUA)	NP_000194.2:n.158+116_158+119del
NM_134425.2:c.576+3768_576+3771del (SLC26A1)	NP_602297.1:n.576+3768_576+3771del
NR_110313.1:n.246+116_246+119del (IDUA)
XM_011513459.1:c.158+116_158+119del (IDUA)	XP_011511761.1:n.158+116_158+119del
XM_011513460.1:c.158+116_158+119del (IDUA)	XP_011511762.1:n.158+116_158+119del
XR_924947.1:n.227+116_227+119del (IDUA)
NM_000203.5:c.158+116_158+119del (IDUA) MANE Select	NP_000194.2:n.158+116_158+119del
XM_017008163.1:c.-1309+116_-1309+119del (IDUA)	XP_016863652.1:n.-1309+116_-1309+119del
NM_134425.3:c.576+3768_576+3771del (SLC26A1)	NP_602297.1:n.576+3768_576+3771del
NM_134425.4:c.576+3768_576+3771del (SLC26A1)	NP_602297.1:n.576+3768_576+3771del