Canonical Allele Identifier: CA414517759
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482814G>T , CM000685.2:g.149482814G>T GRCh38
NC_000023.10:g.148564345G>T , CM000685.1:g.148564345G>T GRCh37
NC_000023.9:g.148372250G>T NCBI36
NG_011900.3:g.27521C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1585C>A MANE Select ENSP00000339801.6:p.Pro529Thr
ENST00000651111.1:c.952C>A ENSP00000498395.1:p.Pro318Thr
ENST00000340855.10:c.1585C>A ENSP00000339801.6:p.Pro529Thr
ENST00000422081.6:c.952C>A ENSP00000477056.1:p.Pro318Thr
NM_000202.6:c.1585C>A NP_000193.1:p.Pro529Thr
NM_001166550.2:c.1315C>A NP_001160022.1:p.Pro439Thr
NM_000202.7:c.1585C>A NP_000193.1:p.Pro529Thr
NM_001166550.3:c.1315C>A NP_001160022.1:p.Pro439Thr
NM_000202.8:c.1585C>A MANE Select NP_000193.1:p.Pro529Thr
NM_001166550.4:c.1315C>A NP_001160022.1:p.Pro439Thr