Canonical Allele Identifier: CA414518998
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 988689
ClinVar RCV Id: RCV001291013
dbSNP Id: rs2089343063

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149487077C>T , CM000685.2:g.149487077C>T GRCh38
NC_000023.10:g.148568608C>T , CM000685.1:g.148568608C>T GRCh37
NC_000023.9:g.148376513C>T NCBI36
NG_011900.3:g.23258G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1028G>A MANE Select ENSP00000339801.6:p.Gly343Glu
ENST00000651111.1:c.395G>A ENSP00000498395.1:p.Gly132Glu
ENST00000340855.10:c.1028G>A ENSP00000339801.6:p.Gly343Glu
ENST00000422081.6:c.395G>A ENSP00000477056.1:p.Gly132Glu
ENST00000441880.1:n.135G>A
NM_000202.6:c.1028G>A NP_000193.1:p.Gly343Glu
NM_001166550.2:c.758G>A NP_001160022.1:p.Gly253Glu
NM_000202.7:c.1028G>A NP_000193.1:p.Gly343Glu
NM_001166550.3:c.758G>A NP_001160022.1:p.Gly253Glu
NM_000202.8:c.1028G>A MANE Select NP_000193.1:p.Gly343Glu
NM_001166550.4:c.758G>A NP_001160022.1:p.Gly253Glu