Canonical Allele Identifier: CA337036002
Gene: IDS HGNC NCBI

Linked Data

dbSNP Id: rs894742419

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490406G>T , CM000685.2:g.149490406G>T GRCh38
NC_000023.10:g.148571937G>T , CM000685.1:g.148571937G>T GRCh37
NC_000023.9:g.148379842G>T NCBI36
NG_011900.3:g.19929C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.914C>A MANE Select ENSP00000339801.6:p.Ser305Ter
ENST00000651111.1:c.281C>A ENSP00000498395.1:p.Ser94Ter
ENST00000340855.10:c.914C>A ENSP00000339801.6:p.Ser305Ter
ENST00000370441.8:c.914C>A ENSP00000359470.4:p.Ser305Ter
ENST00000422081.6:c.281C>A ENSP00000477056.1:p.Ser94Ter
ENST00000441880.1:n.114-3308C>A
ENST00000464251.5:c.840C>A ENSP00000428980.1:n.840C>A
ENST00000466323.5:c.*105C>A ENSP00000418264.1:n.*105C>A
ENST00000490775.5:n.699C>A
NM_000202.6:c.914C>A NP_000193.1:p.Ser305Ter
NM_001166550.2:c.644C>A NP_001160022.1:p.Ser215Ter
NM_006123.4:c.914C>A NP_006114.1:p.Ser305Ter
NR_104128.1:n.1261C>A
NM_000202.7:c.914C>A NP_000193.1:p.Ser305Ter
NM_001166550.3:c.644C>A NP_001160022.1:p.Ser215Ter
NM_000202.8:c.914C>A MANE Select NP_000193.1:p.Ser305Ter
NM_001166550.4:c.644C>A NP_001160022.1:p.Ser215Ter
NM_006123.5:c.914C>A NP_006114.1:p.Ser305Ter
NR_104128.2:n.1213C>A