Canonical Allele Identifier: CA2465010867
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149503378T= , CM000685.2:g.149503378T= GRCh38
NC_000023.10:g.148584908T= , CM000685.1:g.148584908T= GRCh37
NC_000023.9:g.148392813T= NCBI36
NG_011900.3:g.6957A=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.352A= MANE Select ENSP00000339801.6:p.Thr118=
ENST00000651111.1:c.-215-2341A= ENSP00000498395.1:n.-215-2341A=
ENST00000340855.10:c.352A= ENSP00000339801.6:p.Thr118=
ENST00000370441.8:c.352A= ENSP00000359470.4:p.Thr118=
ENST00000422081.6:c.-215-2341A= ENSP00000477056.1:n.-215-2341A=
ENST00000427113.2:n.770-1155A=
ENST00000428056.6:c.352A= ENSP00000390241.2:p.Thr118=
ENST00000441880.1:n.114-16280A=
ENST00000464251.5:c.175A= ENSP00000428980.1:p.Thr59=
ENST00000466323.5:c.352A= ENSP00000418264.1:p.Thr118=
ENST00000490775.5:n.11A=
ENST00000523759.5:n.533-2341A=
NM_000202.6:c.352A= NP_000193.1:p.Thr118=
NM_001166550.2:c.82A= NP_001160022.1:p.Thr28=
NM_006123.4:c.352A= NP_006114.1:p.Thr118=
NR_104128.1:n.569A=
NM_000202.7:c.352A= NP_000193.1:p.Thr118=
NM_001166550.3:c.82A= NP_001160022.1:p.Thr28=
NM_000202.8:c.352A= MANE Select NP_000193.1:p.Thr118=
NM_001166550.4:c.82A= NP_001160022.1:p.Thr28=
NM_006123.5:c.352A= NP_006114.1:p.Thr118=
NR_104128.2:n.521A=