Canonical Allele Identifier: CA2573055126

Gene: IDS

Linked Data

• ClinVar Variation Id: 1326863
• ClinVar RCV Id: RCV001787248
• dbSNP Id: rs2124006012

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487025_149487026insTATTCT , CM000685.2:g.149487025_149487026insTATTCT	GRCh38
NC_000023.10:g.148568556_148568557insTATTCT , CM000685.1:g.148568556_148568557insTATTCT	GRCh37
NC_000023.9:g.148376461_148376462insTATTCT	NCBI36
NG_011900.3:g.23310_23311insGAATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1080_1081insGAATAA
ENST00000651111.1:c.447_448insGAATAA
ENST00000340855.10:c.1080_1081insGAATAA
ENST00000422081.6:c.447_448insGAATAA
ENST00000441880.1:n.187_188insGAATAA
NM_000202.6:c.1080_1081insGAATAA
NM_001166550.2:c.810_811insGAATAA
NM_000202.7:c.1080_1081insGAATAA
NM_001166550.3:c.810_811insGAATAA
NM_000202.8:c.1080_1081insGAATAA
NM_001166550.4:c.810_811insGAATAA