Canonical Allele Identifier: CA2695236646
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498208_149498219del , CM000685.2:g.149498208_149498219del GRCh38
NC_000023.10:g.148579739_148579750del , CM000685.1:g.148579739_148579750del GRCh37
NC_000023.9:g.148387644_148387655del NCBI36
NG_011900.3:g.12117_12128del

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.597_608del MANE Select ENSP00000339801.6:p.Gln200_Glu203del
ENST00000651111.1:c.-37_-26del ENSP00000498395.1:n.-37_-26del
ENST00000340855.10:c.597_608del ENSP00000339801.6:p.Gln200_Glu203del
ENST00000370441.8:c.597_608del ENSP00000359470.4:p.Gln200_Glu203del
ENST00000422081.6:c.-37_-26del ENSP00000477056.1:n.-37_-26del
ENST00000441880.1:n.114-11120_114-11109del
ENST00000464251.5:c.523_534del ENSP00000428980.1:n.523_534del
ENST00000466019.1:n.49_60del
ENST00000466323.5:c.597_608del ENSP00000418264.1:p.Gln200_Glu203del
ENST00000490775.5:n.382_393del
ENST00000523759.5:n.711_722del
NM_000202.6:c.597_608del NP_000193.1:p.Gln200_Glu203del
NM_001166550.2:c.327_338del NP_001160022.1:p.Gln110_Glu113del
NM_006123.4:c.597_608del NP_006114.1:p.Gln200_Glu203del
NR_104128.1:n.814_825del
NM_000202.7:c.597_608del NP_000193.1:p.Gln200_Glu203del
NM_001166550.3:c.327_338del NP_001160022.1:p.Gln110_Glu113del
NM_000202.8:c.597_608del MANE Select NP_000193.1:p.Gln200_Glu203del
NM_001166550.4:c.327_338del NP_001160022.1:p.Gln110_Glu113del
NM_006123.5:c.597_608del NP_006114.1:p.Gln200_Glu203del
NR_104128.2:n.766_777del