Canonical Allele Identifier: CA355946451

Gene: IDUA SLC26A1

Linked Data

• gnomAD v4: 4-987888-G-T
• MyVariant Identifiers: chr4:g.981676G>T (hg19) ; chr4:g.987888G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987888G>T , CM000666.2:g.987888G>T	GRCh38
NC_000004.11:g.981676G>T , CM000666.1:g.981676G>T	GRCh37
NC_000004.10:g.971676G>T	NCBI36
NG_008103.1:g.5892G>T
NG_033042.1:g.10549C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.238G>T (IDUA)	ENSP00000247933.4:p.Val80Phe
ENST00000398516.3:c.*945C>A (SLC26A1) MANE Select	ENSP00000381528.2:n.*945C>A
ENST00000514224.2:c.238G>T (IDUA) MANE Select	ENSP00000425081.2:p.Val80Phe
ENST00000247933.8:c.238G>T (IDUA)	ENSP00000247933.4:p.Val80Phe
ENST00000361661.6:c.*945C>A (SLC26A1)	ENSP00000354721.2:n.*945C>A
ENST00000398520.6:c.576+3240C>A (SLC26A1)	ENSP00000381532.2:n.576+3240C>A
ENST00000502910.5:c.158+646G>T (IDUA)	ENSP00000422952.1:n.158+646G>T
ENST00000504568.5:c.236G>T (IDUA)
ENST00000506561.5:n.247G>T (IDUA)
ENST00000508168.5:n.177+646G>T (IDUA)
ENST00000514698.5:n.199+646G>T (IDUA)
ENST00000622731.4:c.576+3240C>A (SLC26A1)	ENSP00000483506.1:n.576+3240C>A
NM_000203.4:c.238G>T (IDUA)	NP_000194.2:p.Val80Phe
NM_022042.3:c.*945C>A (SLC26A1)	NP_071325.2:n.*945C>A
NM_134425.2:c.576+3240C>A (SLC26A1)	NP_602297.1:n.576+3240C>A
NM_213613.3:c.*945C>A (SLC26A1)	NP_998778.1:n.*945C>A
NR_110313.1:n.326G>T (IDUA)
XM_006713856.2:c.*945C>A (SLC26A1)	XP_006713919.1:n.*945C>A
XM_011513459.1:c.158+646G>T (IDUA)	XP_011511761.1:n.158+646G>T
XM_011513460.1:c.158+646G>T (IDUA)	XP_011511762.1:n.158+646G>T
XM_011513462.1:c.-876G>T (IDUA)	XP_011511764.1:n.-876G>T
XR_924947.1:n.307G>T (IDUA)
NM_000203.5:c.238G>T (IDUA) MANE Select	NP_000194.2:p.Val80Phe
XM_017008163.1:c.-1229G>T (IDUA)	XP_016863652.1:n.-1229G>T
NM_022042.4:c.*945C>A (SLC26A1) MANE Select	NP_071325.2:n.*945C>A
NM_134425.3:c.576+3240C>A (SLC26A1)	NP_602297.1:n.576+3240C>A
NM_213613.4:c.*945C>A (SLC26A1)	NP_998778.1:n.*945C>A
NM_134425.4:c.576+3240C>A (SLC26A1)	NP_602297.1:n.576+3240C>A