Canonical Allele Identifier: CA414518319
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483068A>T , CM000685.2:g.149483068A>T GRCh38
NC_000023.10:g.148564599A>T , CM000685.1:g.148564599A>T GRCh37
NC_000023.9:g.148372504A>T NCBI36
NG_011900.3:g.27267T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1331T>A MANE Select ENSP00000339801.6:p.Phe444Tyr
ENST00000651111.1:c.698T>A ENSP00000498395.1:p.Phe233Tyr
ENST00000340855.10:c.1331T>A ENSP00000339801.6:p.Phe444Tyr
ENST00000422081.6:c.698T>A ENSP00000477056.1:p.Phe233Tyr
NM_000202.6:c.1331T>A NP_000193.1:p.Phe444Tyr
NM_001166550.2:c.1061T>A NP_001160022.1:p.Phe354Tyr
NM_000202.7:c.1331T>A NP_000193.1:p.Phe444Tyr
NM_001166550.3:c.1061T>A NP_001160022.1:p.Phe354Tyr
NM_000202.8:c.1331T>A MANE Select NP_000193.1:p.Phe444Tyr
NM_001166550.4:c.1061T>A NP_001160022.1:p.Phe354Tyr