Canonical Allele Identifier: CA2694909083

Gene: IDS

Linked Data

• gnomAD v4: X-149487143-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487143A>T , CM000685.2:g.149487143A>T	GRCh38
NC_000023.10:g.148568674A>T , CM000685.1:g.148568674A>T	GRCh37
NC_000023.9:g.148376579A>T	NCBI36
NG_011900.3:g.23192T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-45T>A MANE Select	ENSP00000339801.6:n.1007-45T>A
ENST00000651111.1:c.374-45T>A	ENSP00000498395.1:n.374-45T>A
ENST00000340855.10:c.1007-45T>A	ENSP00000339801.6:n.1007-45T>A
ENST00000370441.8:c.*145T>A	ENSP00000359470.4:n.*145T>A
ENST00000422081.6:c.374-45T>A	ENSP00000477056.1:n.374-45T>A
ENST00000441880.1:n.114-45T>A
ENST00000466323.5:c.*368T>A	ENSP00000418264.1:n.*368T>A
NM_000202.6:c.1007-45T>A	NP_000193.1:n.1007-45T>A
NM_001166550.2:c.737-45T>A	NP_001160022.1:n.737-45T>A
NM_006123.4:c.*145T>A	NP_006114.1:n.*145T>A
NR_104128.1:n.1524T>A
NM_000202.7:c.1007-45T>A	NP_000193.1:n.1007-45T>A
NM_001166550.3:c.737-45T>A	NP_001160022.1:n.737-45T>A
NM_000202.8:c.1007-45T>A MANE Select	NP_000193.1:n.1007-45T>A
NM_001166550.4:c.737-45T>A	NP_001160022.1:n.737-45T>A
NM_006123.5:c.*145T>A	NP_006114.1:n.*145T>A
NR_104128.2:n.1476T>A