Canonical Allele Identifier: CA1138320203

Gene: IDS

Linked Data

• gnomAD v3: X-149490733-T-TCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA
• gnomAD v4: X-149490733-T-TCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490733_149490734insCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA , CM000685.2:g.149490733_149490734insCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA	GRCh38
NC_000023.10:g.148572264_148572265insCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA , CM000685.1:g.148572264_148572265insCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA	GRCh37
NC_000023.9:g.148380169_148380170insCAGTCCCTTGAAACACAGGCCCACACATGCTCTGGTAAGGGCCACA	NCBI36
NG_011900.3:g.19601_19602insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG MANE Select	ENSP00000339801.6:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000651111.1:c.247-294_247-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000498395.1:n.247-294_247-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000340855.10:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000339801.6:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000370441.8:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000359470.4:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000422081.6:c.247-294_247-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000477056.1:n.247-294_247-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000441880.1:n.114-3636_114-3635insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG
ENST00000464251.5:c.806-294_806-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000428980.1:n.806-294_806-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000466323.5:c.*71-294_*71-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	ENSP00000418264.1:n.*71-294_*71-293insTGTGGCCCTTACCAGAGCATGTG...
ENST00000490775.5:n.665-294_665-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG
NM_000202.6:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_000193.1:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCC...
NM_001166550.2:c.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_001160022.1:n.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGG...
NM_006123.4:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_006114.1:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCC...
NR_104128.1:n.1227-294_1227-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG
NM_000202.7:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_000193.1:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCC...
NM_001166550.3:c.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_001160022.1:n.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGG...
NM_000202.8:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG MANE Select	NP_000193.1:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCC...
NM_001166550.4:c.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_001160022.1:n.610-294_610-293insTGTGGCCCTTACCAGAGCATGTGTGG...
NM_006123.5:c.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG	NP_006114.1:n.880-294_880-293insTGTGGCCCTTACCAGAGCATGTGTGGGCC...
NR_104128.2:n.1179-294_1179-293insTGTGGCCCTTACCAGAGCATGTGTGGGCCTGTGTTTCAAGGGACTG