Canonical Allele Identifier: CA2465010871
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149503409G= , CM000685.2:g.149503409G= GRCh38
NC_000023.10:g.148584939G= , CM000685.1:g.148584939G= GRCh37
NC_000023.9:g.148392844G= NCBI36
NG_011900.3:g.6926C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.321C= MANE Select ENSP00000339801.6:p.Ser107=
ENST00000651111.1:c.-215-2372C= ENSP00000498395.1:n.-215-2372C=
ENST00000340855.10:c.321C= ENSP00000339801.6:p.Ser107=
ENST00000370441.8:c.321C= ENSP00000359470.4:p.Ser107=
ENST00000422081.6:c.-215-2372C= ENSP00000477056.1:n.-215-2372C=
ENST00000427113.2:n.770-1186C=
ENST00000428056.6:c.321C= ENSP00000390241.2:p.Ser107=
ENST00000441880.1:n.114-16311C=
ENST00000464251.5:c.144C= ENSP00000428980.1:p.Ser48=
ENST00000466323.5:c.321C= ENSP00000418264.1:p.Ser107=
ENST00000523759.5:n.533-2372C=
NM_000202.6:c.321C= NP_000193.1:p.Ser107=
NM_001166550.2:c.51C= NP_001160022.1:p.Ser17=
NM_006123.4:c.321C= NP_006114.1:p.Ser107=
NR_104128.1:n.538C=
NM_000202.7:c.321C= NP_000193.1:p.Ser107=
NM_001166550.3:c.51C= NP_001160022.1:p.Ser17=
NM_000202.8:c.321C= MANE Select NP_000193.1:p.Ser107=
NM_001166550.4:c.51C= NP_001160022.1:p.Ser17=
NM_006123.5:c.321C= NP_006114.1:p.Ser107=
NR_104128.2:n.490C=