Canonical Allele Identifier: CA2465009231
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498212G= , CM000685.2:g.149498212G= GRCh38
NC_000023.10:g.148579743G= , CM000685.1:g.148579743G= GRCh37
NC_000023.9:g.148387648G= NCBI36
NG_011900.3:g.12123C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.603C= MANE Select ENSP00000339801.6:p.Ser201=
ENST00000651111.1:c.-31C= ENSP00000498395.1:n.-31C=
ENST00000340855.10:c.603C= ENSP00000339801.6:p.Ser201=
ENST00000370441.8:c.603C= ENSP00000359470.4:p.Ser201=
ENST00000422081.6:c.-31C= ENSP00000477056.1:n.-31C=
ENST00000441880.1:n.114-11114C=
ENST00000464251.5:c.529C= ENSP00000428980.1:n.529C=
ENST00000466019.1:n.55C=
ENST00000466323.5:c.603C= ENSP00000418264.1:p.Ser201=
ENST00000490775.5:n.388C=
ENST00000523759.5:n.717C=
NM_000202.6:c.603C= NP_000193.1:p.Ser201=
NM_001166550.2:c.333C= NP_001160022.1:p.Ser111=
NM_006123.4:c.603C= NP_006114.1:p.Ser201=
NR_104128.1:n.820C=
NM_000202.7:c.603C= NP_000193.1:p.Ser201=
NM_001166550.3:c.333C= NP_001160022.1:p.Ser111=
NM_000202.8:c.603C= MANE Select NP_000193.1:p.Ser201=
NM_001166550.4:c.333C= NP_001160022.1:p.Ser111=
NM_006123.5:c.603C= NP_006114.1:p.Ser201=
NR_104128.2:n.772C=