Canonical Allele Identifier: CA2579719107
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483213del , CM000685.2:g.149483213del GRCh38
NC_000023.10:g.148564744del , CM000685.1:g.148564744del GRCh37
NC_000023.9:g.148372649del NCBI36
NG_011900.3:g.27122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1186del MANE Select ENSP00000339801.6:p.Gln396AsnfsTer?
ENST00000651111.1:c.553del ENSP00000498395.1:p.Gln185AsnfsTer?
ENST00000340855.10:c.1186del ENSP00000339801.6:p.Gln396AsnfsTer?
ENST00000422081.6:c.553del ENSP00000477056.1:p.Gln185AsnfsTer?
ENST00000441880.1:n.293del
NM_000202.6:c.1186del NP_000193.1:p.Gln396AsnfsTer?
NM_001166550.2:c.916del NP_001160022.1:p.Gln306AsnfsTer?
NM_000202.7:c.1186del NP_000193.1:p.Gln396AsnfsTer?
NM_001166550.3:c.916del NP_001160022.1:p.Gln306AsnfsTer?
NM_000202.8:c.1186del MANE Select NP_000193.1:p.Gln396AsnfsTer?
NM_001166550.4:c.916del NP_001160022.1:p.Gln306AsnfsTer?