Canonical Allele Identifier: CA2580101611
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1710487
ClinVar RCV Id: RCV002291494

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482949_149483122del , CM000685.2:g.149482949_149483122del GRCh38
NC_000023.10:g.148564480_148564653del , CM000685.1:g.148564480_148564653del GRCh37
NC_000023.9:g.148372385_148372558del NCBI36
NG_011900.3:g.27213_27386del

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1277_1450del MANE Select ENSP00000339801.6:p.Ser426_Asp484delinsTy...
ENST00000651111.1:c.644_817del ENSP00000498395.1:p.Ser215_Asp273delinsTy...
ENST00000340855.10:c.1277_1450del ENSP00000339801.6:p.Ser426_Asp484delinsTy...
ENST00000422081.6:c.644_817del ENSP00000477056.1:p.Ser215_Asp273delinsTy...
NM_000202.6:c.1277_1450del NP_000193.1:p.Ser426_Asp484delinsTyr
NM_001166550.2:c.1007_1180del NP_001160022.1:p.Ser336_Asp394delinsTyr
NM_000202.7:c.1277_1450del NP_000193.1:p.Ser426_Asp484delinsTyr
NM_001166550.3:c.1007_1180del NP_001160022.1:p.Ser336_Asp394delinsTyr
NM_000202.8:c.1277_1450del MANE Select NP_000193.1:p.Ser426_Asp484delinsTyr
NM_001166550.4:c.1007_1180del NP_001160022.1:p.Ser336_Asp394delinsTyr