Canonical Allele Identifier: CA414520354
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490407A>C , CM000685.2:g.149490407A>C GRCh38
NC_000023.10:g.148571938A>C , CM000685.1:g.148571938A>C GRCh37
NC_000023.9:g.148379843A>C NCBI36
NG_011900.3:g.19928T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.913T>G MANE Select ENSP00000339801.6:p.Ser305Ala
ENST00000651111.1:c.280T>G ENSP00000498395.1:p.Ser94Ala
ENST00000340855.10:c.913T>G ENSP00000339801.6:p.Ser305Ala
ENST00000370441.8:c.913T>G ENSP00000359470.4:p.Ser305Ala
ENST00000422081.6:c.280T>G ENSP00000477056.1:p.Ser94Ala
ENST00000441880.1:n.114-3309T>G
ENST00000464251.5:c.839T>G ENSP00000428980.1:n.839T>G
ENST00000466323.5:c.*104T>G ENSP00000418264.1:n.*104T>G
ENST00000490775.5:n.698T>G
NM_000202.6:c.913T>G NP_000193.1:p.Ser305Ala
NM_001166550.2:c.643T>G NP_001160022.1:p.Ser215Ala
NM_006123.4:c.913T>G NP_006114.1:p.Ser305Ala
NR_104128.1:n.1260T>G
NM_000202.7:c.913T>G NP_000193.1:p.Ser305Ala
NM_001166550.3:c.643T>G NP_001160022.1:p.Ser215Ala
NM_000202.8:c.913T>G MANE Select NP_000193.1:p.Ser305Ala
NM_001166550.4:c.643T>G NP_001160022.1:p.Ser215Ala
NM_006123.5:c.913T>G NP_006114.1:p.Ser305Ala
NR_104128.2:n.1212T>G