Canonical Allele Identifier: CA2695236515
Gene: IDS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483081dup , CM000685.2:g.149483081dup GRCh38
NC_000023.10:g.148564612dup , CM000685.1:g.148564612dup GRCh37
NC_000023.9:g.148372517dup NCBI36
NG_011900.3:g.27255dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1319dup MANE Select ENSP00000339801.6:p.His441AlafsTer6
ENST00000651111.1:c.686dup ENSP00000498395.1:p.His230AlafsTer6
ENST00000340855.10:c.1319dup ENSP00000339801.6:p.His441AlafsTer6
ENST00000422081.6:c.686dup ENSP00000477056.1:p.His230AlafsTer6
NM_000202.6:c.1319dup NP_000193.1:p.His441AlafsTer6
NM_001166550.2:c.1049dup NP_001160022.1:p.His351AlafsTer6
NM_000202.7:c.1319dup NP_000193.1:p.His441AlafsTer6
NM_001166550.3:c.1049dup NP_001160022.1:p.His351AlafsTer6
NM_000202.8:c.1319dup MANE Select NP_000193.1:p.His441AlafsTer6
NM_001166550.4:c.1049dup NP_001160022.1:p.His351AlafsTer6
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