Canonical Allele Identifier: CA414517990
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482915A>C , CM000685.2:g.149482915A>C GRCh38
NC_000023.10:g.148564446A>C , CM000685.1:g.148564446A>C GRCh37
NC_000023.9:g.148372351A>C NCBI36
NG_011900.3:g.27420T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1484T>G MANE Select ENSP00000339801.6:p.Ile495Arg
ENST00000651111.1:c.851T>G ENSP00000498395.1:p.Ile284Arg
ENST00000340855.10:c.1484T>G ENSP00000339801.6:p.Ile495Arg
ENST00000422081.6:c.851T>G ENSP00000477056.1:p.Ile284Arg
NM_000202.6:c.1484T>G NP_000193.1:p.Ile495Arg
NM_001166550.2:c.1214T>G NP_001160022.1:p.Ile405Arg
NM_000202.7:c.1484T>G NP_000193.1:p.Ile495Arg
NM_001166550.3:c.1214T>G NP_001160022.1:p.Ile405Arg
NM_000202.8:c.1484T>G MANE Select NP_000193.1:p.Ile495Arg
NM_001166550.4:c.1214T>G NP_001160022.1:p.Ile405Arg