Canonical Allele Identifier: CA2830563717
Gene: IDS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482965del , CM000685.2:g.149482965del GRCh38
NC_000023.10:g.148564496del , CM000685.1:g.148564496del GRCh37
NC_000023.9:g.148372401del NCBI36
NG_011900.3:g.27370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1434del MANE Select ENSP00000339801.6:p.Asp478GlufsTer5
ENST00000651111.1:c.801del ENSP00000498395.1:p.Asp267GlufsTer5
ENST00000340855.10:c.1434del ENSP00000339801.6:p.Asp478GlufsTer5
ENST00000422081.6:c.801del ENSP00000477056.1:p.Asp267GlufsTer5
NM_000202.6:c.1434del NP_000193.1:p.Asp478GlufsTer5
NM_001166550.2:c.1164del NP_001160022.1:p.Asp388GlufsTer5
NM_000202.7:c.1434del NP_000193.1:p.Asp478GlufsTer5
NM_001166550.3:c.1164del NP_001160022.1:p.Asp388GlufsTer5
NM_000202.8:c.1434del MANE Select NP_000193.1:p.Asp478GlufsTer5
NM_001166550.4:c.1164del NP_001160022.1:p.Asp388GlufsTer5
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