Canonical Allele Identifier: CA2465006786
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490387G= , CM000685.2:g.149490387G= GRCh38
NC_000023.10:g.148571918G= , CM000685.1:g.148571918G= GRCh37
NC_000023.9:g.148379823G= NCBI36
NG_011900.3:g.19948C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.933C= MANE Select ENSP00000339801.6:p.Val311=
ENST00000651111.1:c.300C= ENSP00000498395.1:p.Val100=
ENST00000340855.10:c.933C= ENSP00000339801.6:p.Val311=
ENST00000370441.8:c.933C= ENSP00000359470.4:p.Val311=
ENST00000422081.6:c.300C= ENSP00000477056.1:p.Val100=
ENST00000441880.1:n.114-3289C=
ENST00000464251.5:c.859C= ENSP00000428980.1:n.859C=
ENST00000466323.5:c.*124C= ENSP00000418264.1:n.*124C=
ENST00000490775.5:n.718C=
NM_000202.6:c.933C= NP_000193.1:p.Val311=
NM_001166550.2:c.663C= NP_001160022.1:p.Val221=
NM_006123.4:c.933C= NP_006114.1:p.Val311=
NR_104128.1:n.1280C=
NM_000202.7:c.933C= NP_000193.1:p.Val311=
NM_001166550.3:c.663C= NP_001160022.1:p.Val221=
NM_000202.8:c.933C= MANE Select NP_000193.1:p.Val311=
NM_001166550.4:c.663C= NP_001160022.1:p.Val221=
NM_006123.5:c.933C= NP_006114.1:p.Val311=
NR_104128.2:n.1232C=