Canonical Allele Identifier: CA2695236658
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498251_149498266dup , CM000685.2:g.149498251_149498266dup GRCh38
NC_000023.10:g.148579782_148579797dup , CM000685.1:g.148579782_148579797dup GRCh37
NC_000023.9:g.148387687_148387702dup NCBI36
NG_011900.3:g.12069_12084dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.549_564dup MANE Select ENSP00000339801.6:p.Asp190ProfsTer14
ENST00000651111.1:c.-85_-70dup ENSP00000498395.1:n.-85_-70dup
ENST00000340855.10:c.549_564dup ENSP00000339801.6:p.Asp190ProfsTer14
ENST00000370441.8:c.549_564dup ENSP00000359470.4:p.Asp190ProfsTer14
ENST00000422081.6:c.-85_-70dup ENSP00000477056.1:n.-85_-70dup
ENST00000441880.1:n.114-11168_114-11153dup
ENST00000464251.5:c.475_490dup ENSP00000428980.1:n.475_490dup
ENST00000466019.1:n.1_16dup
ENST00000466323.5:c.549_564dup ENSP00000418264.1:p.Asp190ProfsTer14
ENST00000490775.5:n.334_349dup
ENST00000523759.5:n.663_678dup
NM_000202.6:c.549_564dup NP_000193.1:p.Asp190ProfsTer14
NM_001166550.2:c.279_294dup NP_001160022.1:p.Asp100ProfsTer14
NM_006123.4:c.549_564dup NP_006114.1:p.Asp190ProfsTer14
NR_104128.1:n.766_781dup
NM_000202.7:c.549_564dup NP_000193.1:p.Asp190ProfsTer14
NM_001166550.3:c.279_294dup NP_001160022.1:p.Asp100ProfsTer14
NM_000202.8:c.549_564dup MANE Select NP_000193.1:p.Asp190ProfsTer14
NM_001166550.4:c.279_294dup NP_001160022.1:p.Asp100ProfsTer14
NM_006123.5:c.549_564dup NP_006114.1:p.Asp190ProfsTer14
NR_104128.2:n.718_733dup