Canonical Allele Identifier: CA414518047
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482942T>G , CM000685.2:g.149482942T>G GRCh38
NC_000023.10:g.148564473T>G , CM000685.1:g.148564473T>G GRCh37
NC_000023.9:g.148372378T>G NCBI36
NG_011900.3:g.27393A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1457A>C MANE Select ENSP00000339801.6:p.Lys486Thr
ENST00000651111.1:c.824A>C ENSP00000498395.1:p.Lys275Thr
ENST00000340855.10:c.1457A>C ENSP00000339801.6:p.Lys486Thr
ENST00000422081.6:c.824A>C ENSP00000477056.1:p.Lys275Thr
NM_000202.6:c.1457A>C NP_000193.1:p.Lys486Thr
NM_001166550.2:c.1187A>C NP_001160022.1:p.Lys396Thr
NM_000202.7:c.1457A>C NP_000193.1:p.Lys486Thr
NM_001166550.3:c.1187A>C NP_001160022.1:p.Lys396Thr
NM_000202.8:c.1457A>C MANE Select NP_000193.1:p.Lys486Thr
NM_001166550.4:c.1187A>C NP_001160022.1:p.Lys396Thr