Canonical Allele Identifier: CA2695236659
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498257del , CM000685.2:g.149498257del GRCh38
NC_000023.10:g.148579788del , CM000685.1:g.148579788del GRCh37
NC_000023.9:g.148387693del NCBI36
NG_011900.3:g.12079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.559del MANE Select ENSP00000339801.6:p.Asp187MetfsTer26
ENST00000651111.1:c.-75del ENSP00000498395.1:n.-75del
ENST00000340855.10:c.559del ENSP00000339801.6:p.Asp187MetfsTer26
ENST00000370441.8:c.559del ENSP00000359470.4:p.Asp187MetfsTer26
ENST00000422081.6:c.-75del ENSP00000477056.1:n.-75del
ENST00000441880.1:n.114-11158del
ENST00000464251.5:c.485del ENSP00000428980.1:n.485del
ENST00000466019.1:n.11del
ENST00000466323.5:c.559del ENSP00000418264.1:p.Asp187MetfsTer26
ENST00000490775.5:n.344del
ENST00000523759.5:n.673del
NM_000202.6:c.559del NP_000193.1:p.Asp187MetfsTer26
NM_001166550.2:c.289del NP_001160022.1:p.Asp97MetfsTer26
NM_006123.4:c.559del NP_006114.1:p.Asp187MetfsTer26
NR_104128.1:n.776del
NM_000202.7:c.559del NP_000193.1:p.Asp187MetfsTer26
NM_001166550.3:c.289del NP_001160022.1:p.Asp97MetfsTer26
NM_000202.8:c.559del MANE Select NP_000193.1:p.Asp187MetfsTer26
NM_001166550.4:c.289del NP_001160022.1:p.Asp97MetfsTer26
NM_006123.5:c.559del NP_006114.1:p.Asp187MetfsTer26
NR_104128.2:n.728del