Canonical Allele Identifier: CA2465004000
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482981G= , CM000685.2:g.149482981G= GRCh38
NC_000023.10:g.148564512G= , CM000685.1:g.148564512G= GRCh37
NC_000023.9:g.148372417G= NCBI36
NG_011900.3:g.27354C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1418C= MANE Select ENSP00000339801.6:p.Pro473=
ENST00000651111.1:c.785C= ENSP00000498395.1:p.Pro262=
ENST00000340855.10:c.1418C= ENSP00000339801.6:p.Pro473=
ENST00000422081.6:c.785C= ENSP00000477056.1:p.Pro262=
NM_000202.6:c.1418C= NP_000193.1:p.Pro473=
NM_001166550.2:c.1148C= NP_001160022.1:p.Pro383=
NM_000202.7:c.1418C= NP_000193.1:p.Pro473=
NM_001166550.3:c.1148C= NP_001160022.1:p.Pro383=
NM_000202.8:c.1418C= MANE Select NP_000193.1:p.Pro473=
NM_001166550.4:c.1148C= NP_001160022.1:p.Pro383=