Canonical Allele Identifier: CA1138320099
Gene: IDS HGNC NCBI

Linked Data

dbSNP Id: rs2089382003

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490521A>C , CM000685.2:g.149490521A>C GRCh38
NC_000023.10:g.148572052A>C , CM000685.1:g.148572052A>C GRCh37
NC_000023.9:g.148379957A>C NCBI36
NG_011900.3:g.19814T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.880-81T>G MANE Select ENSP00000339801.6:n.880-81T>G
ENST00000651111.1:c.247-81T>G ENSP00000498395.1:n.247-81T>G
ENST00000340855.10:c.880-81T>G ENSP00000339801.6:n.880-81T>G
ENST00000370441.8:c.880-81T>G ENSP00000359470.4:n.880-81T>G
ENST00000422081.6:c.247-81T>G ENSP00000477056.1:n.247-81T>G
ENST00000441880.1:n.114-3423T>G
ENST00000464251.5:c.806-81T>G ENSP00000428980.1:n.806-81T>G
ENST00000466323.5:c.*71-81T>G ENSP00000418264.1:n.*71-81T>G
ENST00000490775.5:n.665-81T>G
NM_000202.6:c.880-81T>G NP_000193.1:n.880-81T>G
NM_001166550.2:c.610-81T>G NP_001160022.1:n.610-81T>G
NM_006123.4:c.880-81T>G NP_006114.1:n.880-81T>G
NR_104128.1:n.1227-81T>G
NM_000202.7:c.880-81T>G NP_000193.1:n.880-81T>G
NM_001166550.3:c.610-81T>G NP_001160022.1:n.610-81T>G
NM_000202.8:c.880-81T>G MANE Select NP_000193.1:n.880-81T>G
NM_001166550.4:c.610-81T>G NP_001160022.1:n.610-81T>G
NM_006123.5:c.880-81T>G NP_006114.1:n.880-81T>G
NR_104128.2:n.1179-81T>G