Canonical Allele Identifier: CA2465010056
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149500903_149500905delinsAGG , CM000685.2:g.149500903_149500905delinsAGG GRCh38
NC_000023.10:g.148582434_148582436delinsAGG , CM000685.1:g.148582434_148582436delinsAGG GRCh37
NC_000023.9:g.148390339_148390341delinsAGG NCBI36
NG_011900.3:g.9430_9432delinsCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.507+44_507+46delinsCCT MANE Select ENSP00000339801.6:n.507+44_507+46delinsCC...
ENST00000651111.1:c.-127+44_-127+46delinsCCT ENSP00000498395.1:n.-127+44_-127+46delins...
ENST00000340855.10:c.507+44_507+46delinsCCT ENSP00000339801.6:n.507+44_507+46delinsCC...
ENST00000370441.8:c.507+44_507+46delinsCCT ENSP00000359470.4:n.507+44_507+46delinsCC...
ENST00000422081.6:c.-127+44_-127+46delinsCCT ENSP00000477056.1:n.-127+44_-127+46delins...
ENST00000441880.1:n.114-13807_114-13805delinsCCT
ENST00000464251.5:c.433+44_433+46delinsCCT ENSP00000428980.1:n.433+44_433+46delinsCC...
ENST00000466323.5:c.507+44_507+46delinsCCT ENSP00000418264.1:n.507+44_507+46delinsCC...
ENST00000490775.5:n.166+44_166+46delinsCCT
ENST00000523759.5:n.621+44_621+46delinsCCT
NM_000202.6:c.507+44_507+46delinsCCT NP_000193.1:n.507+44_507+46delinsCCT
NM_001166550.2:c.237+44_237+46delinsCCT NP_001160022.1:n.237+44_237+46delinsCCT
NM_006123.4:c.507+44_507+46delinsCCT NP_006114.1:n.507+44_507+46delinsCCT
NR_104128.1:n.724+44_724+46delinsCCT
NM_000202.7:c.507+44_507+46delinsCCT NP_000193.1:n.507+44_507+46delinsCCT
NM_001166550.3:c.237+44_237+46delinsCCT NP_001160022.1:n.237+44_237+46delinsCCT
NM_000202.8:c.507+44_507+46delinsCCT MANE Select NP_000193.1:n.507+44_507+46delinsCCT
NM_001166550.4:c.237+44_237+46delinsCCT NP_001160022.1:n.237+44_237+46delinsCCT
NM_006123.5:c.507+44_507+46delinsCCT NP_006114.1:n.507+44_507+46delinsCCT
NR_104128.2:n.676+44_676+46delinsCCT