Canonical Allele Identifier: CA2465005575
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149487012C= , CM000685.2:g.149487012C= GRCh38
NC_000023.10:g.148568543C= , CM000685.1:g.148568543C= GRCh37
NC_000023.9:g.148376448C= NCBI36
NG_011900.3:g.23323G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1093G= MANE Select ENSP00000339801.6:p.Gly365=
ENST00000651111.1:c.460G= ENSP00000498395.1:p.Gly154=
ENST00000340855.10:c.1093G= ENSP00000339801.6:p.Gly365=
ENST00000422081.6:c.460G= ENSP00000477056.1:p.Gly154=
ENST00000441880.1:n.200G=
NM_000202.6:c.1093G= NP_000193.1:p.Gly365=
NM_001166550.2:c.823G= NP_001160022.1:p.Gly275=
NM_000202.7:c.1093G= NP_000193.1:p.Gly365=
NM_001166550.3:c.823G= NP_001160022.1:p.Gly275=
NM_000202.8:c.1093G= MANE Select NP_000193.1:p.Gly365=
NM_001166550.4:c.823G= NP_001160022.1:p.Gly275=