Canonical Allele Identifier: CA2541757428
Gene: IDS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490311del , CM000685.2:g.149490311del GRCh38
NC_000023.10:g.148571842del , CM000685.1:g.148571842del GRCh37
NC_000023.9:g.148379747del NCBI36
NG_011900.3:g.20025del

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1006+4del MANE Select ENSP00000339801.6:n.1006+4del
ENST00000651111.1:c.373+4del ENSP00000498395.1:n.373+4del
ENST00000340855.10:c.1006+4del ENSP00000339801.6:n.1006+4del
ENST00000370441.8:c.1006+4del ENSP00000359470.4:n.1006+4del
ENST00000422081.6:c.373+4del ENSP00000477056.1:n.373+4del
ENST00000441880.1:n.114-3212del
ENST00000464251.5:c.932+4del ENSP00000428980.1:n.932+4del
ENST00000466323.5:c.*197+4del ENSP00000418264.1:n.*197+4del
ENST00000490775.5:n.791+4del
NM_000202.6:c.1006+4del NP_000193.1:n.1006+4del
NM_001166550.2:c.736+4del NP_001160022.1:n.736+4del
NM_006123.4:c.1006+4del NP_006114.1:n.1006+4del
NR_104128.1:n.1353+4del
NM_000202.7:c.1006+4del NP_000193.1:n.1006+4del
NM_001166550.3:c.736+4del NP_001160022.1:n.736+4del
NM_000202.8:c.1006+4del MANE Select NP_000193.1:n.1006+4del
NM_001166550.4:c.736+4del NP_001160022.1:n.736+4del
NM_006123.5:c.1006+4del NP_006114.1:n.1006+4del
NR_104128.2:n.1305+4del
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