Canonical Allele Identifier: CA2695236582
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149503354dup , CM000685.2:g.149503354dup GRCh38
NC_000023.10:g.148584884dup , CM000685.1:g.148584884dup GRCh37
NC_000023.9:g.148392789dup NCBI36
NG_011900.3:g.6982dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.377dup MANE Select ENSP00000339801.6:p.Asn126LysfsTer19
ENST00000651111.1:c.-215-2316dup ENSP00000498395.1:n.-215-2316dup
ENST00000340855.10:c.377dup ENSP00000339801.6:p.Asn126LysfsTer19
ENST00000370441.8:c.377dup ENSP00000359470.4:p.Asn126LysfsTer19
ENST00000422081.6:c.-215-2316dup ENSP00000477056.1:n.-215-2316dup
ENST00000427113.2:n.770-1130dup
ENST00000428056.6:c.377dup ENSP00000390241.2:p.Asn126LysfsTer31
ENST00000441880.1:n.114-16255dup
ENST00000464251.5:c.200dup ENSP00000428980.1:p.Asn67LysfsTer24
ENST00000466323.5:c.377dup ENSP00000418264.1:p.Asn126LysfsTer19
ENST00000490775.5:n.36dup
ENST00000523759.5:n.533-2316dup
NM_000202.6:c.377dup NP_000193.1:p.Asn126LysfsTer19
NM_001166550.2:c.107dup NP_001160022.1:p.Asn36LysfsTer19
NM_006123.4:c.377dup NP_006114.1:p.Asn126LysfsTer19
NR_104128.1:n.594dup
NM_000202.7:c.377dup NP_000193.1:p.Asn126LysfsTer19
NM_001166550.3:c.107dup NP_001160022.1:p.Asn36LysfsTer19
NM_000202.8:c.377dup MANE Select NP_000193.1:p.Asn126LysfsTer19
NM_001166550.4:c.107dup NP_001160022.1:p.Asn36LysfsTer19
NM_006123.5:c.377dup NP_006114.1:p.Asn126LysfsTer19
NR_104128.2:n.546dup