Canonical Allele Identifier: CA2465005540
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149486932C= , CM000685.2:g.149486932C= GRCh38
NC_000023.10:g.148568463C= , CM000685.1:g.148568463C= GRCh37
NC_000023.9:g.148376368C= NCBI36
NG_011900.3:g.23403G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1173G= MANE Select ENSP00000339801.6:p.Met391=
ENST00000651111.1:c.540G= ENSP00000498395.1:p.Met180=
ENST00000340855.10:c.1173G= ENSP00000339801.6:p.Met391=
ENST00000422081.6:c.540G= ENSP00000477056.1:p.Met180=
ENST00000441880.1:n.280G=
NM_000202.6:c.1173G= NP_000193.1:p.Met391=
NM_001166550.2:c.903G= NP_001160022.1:p.Met301=
NM_000202.7:c.1173G= NP_000193.1:p.Met391=
NM_001166550.3:c.903G= NP_001160022.1:p.Met301=
NM_000202.8:c.1173G= MANE Select NP_000193.1:p.Met391=
NM_001166550.4:c.903G= NP_001160022.1:p.Met301=