Canonical Allele Identifier: CA2465006790
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490399C= , CM000685.2:g.149490399C= GRCh38
NC_000023.10:g.148571930C= , CM000685.1:g.148571930C= GRCh37
NC_000023.9:g.148379835C= NCBI36
NG_011900.3:g.19936G=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.921G= MANE Select ENSP00000339801.6:p.Leu307=
ENST00000651111.1:c.288G= ENSP00000498395.1:p.Leu96=
ENST00000340855.10:c.921G= ENSP00000339801.6:p.Leu307=
ENST00000370441.8:c.921G= ENSP00000359470.4:p.Leu307=
ENST00000422081.6:c.288G= ENSP00000477056.1:p.Leu96=
ENST00000441880.1:n.114-3301G=
ENST00000464251.5:c.847G= ENSP00000428980.1:n.847G=
ENST00000466323.5:c.*112G= ENSP00000418264.1:n.*112G=
ENST00000490775.5:n.706G=
NM_000202.6:c.921G= NP_000193.1:p.Leu307=
NM_001166550.2:c.651G= NP_001160022.1:p.Leu217=
NM_006123.4:c.921G= NP_006114.1:p.Leu307=
NR_104128.1:n.1268G=
NM_000202.7:c.921G= NP_000193.1:p.Leu307=
NM_001166550.3:c.651G= NP_001160022.1:p.Leu217=
NM_000202.8:c.921G= MANE Select NP_000193.1:p.Leu307=
NM_001166550.4:c.651G= NP_001160022.1:p.Leu217=
NM_006123.5:c.921G= NP_006114.1:p.Leu307=
NR_104128.2:n.1220G=