Canonical Allele Identifier: CA414518098
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482963T>G , CM000685.2:g.149482963T>G GRCh38
NC_000023.10:g.148564494T>G , CM000685.1:g.148564494T>G GRCh37
NC_000023.9:g.148372399T>G NCBI36
NG_011900.3:g.27372A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1436A>C MANE Select ENSP00000339801.6:p.Lys479Thr
ENST00000651111.1:c.803A>C ENSP00000498395.1:p.Lys268Thr
ENST00000340855.10:c.1436A>C ENSP00000339801.6:p.Lys479Thr
ENST00000422081.6:c.803A>C ENSP00000477056.1:p.Lys268Thr
NM_000202.6:c.1436A>C NP_000193.1:p.Lys479Thr
NM_001166550.2:c.1166A>C NP_001160022.1:p.Lys389Thr
NM_000202.7:c.1436A>C NP_000193.1:p.Lys479Thr
NM_001166550.3:c.1166A>C NP_001160022.1:p.Lys389Thr
NM_000202.8:c.1436A>C MANE Select NP_000193.1:p.Lys479Thr
NM_001166550.4:c.1166A>C NP_001160022.1:p.Lys389Thr