Canonical Allele Identifier: CA2465005529
Gene: IDS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149486896A= , CM000685.2:g.149486896A= GRCh38
NC_000023.10:g.148568427A= , CM000685.1:g.148568427A= GRCh37
NC_000023.9:g.148376332A= NCBI36
NG_011900.3:g.23439T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1180+29T= MANE Select ENSP00000339801.6:n.1180+29T=
ENST00000651111.1:c.547+29T= ENSP00000498395.1:n.547+29T=
ENST00000340855.10:c.1180+29T= ENSP00000339801.6:n.1180+29T=
ENST00000422081.6:c.547+29T= ENSP00000477056.1:n.547+29T=
ENST00000441880.1:n.287+29T=
NM_000202.6:c.1180+29T= NP_000193.1:n.1180+29T=
NM_001166550.2:c.910+29T= NP_001160022.1:n.910+29T=
NM_000202.7:c.1180+29T= NP_000193.1:n.1180+29T=
NM_001166550.3:c.910+29T= NP_001160022.1:n.910+29T=
NM_000202.8:c.1180+29T= MANE Select NP_000193.1:n.1180+29T=
NM_001166550.4:c.910+29T= NP_001160022.1:n.910+29T=
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