Canonical Allele Identifier: CA2465010949
Gene: IDS HGNC NCBI

Linked Data

dbSNP Id: rs2089498766

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149503620A>G , CM000685.2:g.149503620A>G GRCh38
NC_000023.10:g.148585150A>G , CM000685.1:g.148585150A>G GRCh37
NC_000023.9:g.148393054A>G NCBI36
NG_011900.3:g.6715T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.241-131T>C MANE Select ENSP00000339801.6:n.241-131T>C
ENST00000651111.1:c.-215-2583T>C ENSP00000498395.1:n.-215-2583T>C
ENST00000340855.10:c.241-131T>C ENSP00000339801.6:n.241-131T>C
ENST00000370441.8:c.241-131T>C ENSP00000359470.4:n.241-131T>C
ENST00000422081.6:c.-215-2583T>C ENSP00000477056.1:n.-215-2583T>C
ENST00000427113.2:n.770-1397T>C
ENST00000428056.6:c.241-131T>C ENSP00000390241.2:n.241-131T>C
ENST00000441880.1:n.114-16522T>C
ENST00000464251.5:c.64-131T>C ENSP00000428980.1:n.64-131T>C
ENST00000466323.5:c.241-131T>C ENSP00000418264.1:n.241-131T>C
ENST00000521702.1:c.241-131T>C ENSP00000429745.1:n.241-131T>C
ENST00000523759.5:n.533-2583T>C
NM_000202.6:c.241-131T>C NP_000193.1:n.241-131T>C
NM_001166550.2:c.15-175T>C NP_001160022.1:n.15-175T>C
NM_006123.4:c.241-131T>C NP_006114.1:n.241-131T>C
NR_104128.1:n.458-131T>C
NM_000202.7:c.241-131T>C NP_000193.1:n.241-131T>C
NM_001166550.3:c.15-175T>C NP_001160022.1:n.15-175T>C
NM_000202.8:c.241-131T>C MANE Select NP_000193.1:n.241-131T>C
NM_001166550.4:c.15-175T>C NP_001160022.1:n.15-175T>C
NM_006123.5:c.241-131T>C NP_006114.1:n.241-131T>C
NR_104128.2:n.410-131T>C