Canonical Allele Identifier: CA2739146811
Gene: IDS HGNC NCBI

Linked Data

dbSNP Id: rs2124064158

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149503629dup , CM000685.2:g.149503629dup GRCh38
NC_000023.10:g.148585159dup , CM000685.1:g.148585159dup GRCh37
NC_000023.9:g.148393063dup NCBI36
NG_011900.3:g.6706dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.241-140dup MANE Select ENSP00000339801.6:n.241-140dup
ENST00000651111.1:c.-215-2592dup ENSP00000498395.1:n.-215-2592dup
ENST00000340855.10:c.241-140dup ENSP00000339801.6:n.241-140dup
ENST00000370441.8:c.241-140dup ENSP00000359470.4:n.241-140dup
ENST00000422081.6:c.-215-2592dup ENSP00000477056.1:n.-215-2592dup
ENST00000427113.2:n.770-1406dup
ENST00000428056.6:c.241-140dup ENSP00000390241.2:n.241-140dup
ENST00000441880.1:n.114-16531dup
ENST00000464251.5:c.64-140dup ENSP00000428980.1:n.64-140dup
ENST00000466323.5:c.241-140dup ENSP00000418264.1:n.241-140dup
ENST00000521702.1:c.241-140dup ENSP00000429745.1:n.241-140dup
ENST00000523759.5:n.533-2592dup
NM_000202.6:c.241-140dup NP_000193.1:n.241-140dup
NM_001166550.2:c.15-184dup NP_001160022.1:n.15-184dup
NM_006123.4:c.241-140dup NP_006114.1:n.241-140dup
NR_104128.1:n.458-140dup
NM_000202.7:c.241-140dup NP_000193.1:n.241-140dup
NM_001166550.3:c.15-184dup NP_001160022.1:n.15-184dup
NM_000202.8:c.241-140dup MANE Select NP_000193.1:n.241-140dup
NM_001166550.4:c.15-184dup NP_001160022.1:n.15-184dup
NM_006123.5:c.241-140dup NP_006114.1:n.241-140dup
NR_104128.2:n.410-140dup