Canonical Allele Identifier: CA2465006785
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490386C= , CM000685.2:g.149490386C= GRCh38
NC_000023.10:g.148571917C= , CM000685.1:g.148571917C= GRCh37
NC_000023.9:g.148379822C= NCBI36
NG_011900.3:g.19949G=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.934G= MANE Select ENSP00000339801.6:p.Gly312=
ENST00000651111.1:c.301G= ENSP00000498395.1:p.Gly101=
ENST00000340855.10:c.934G= ENSP00000339801.6:p.Gly312=
ENST00000370441.8:c.934G= ENSP00000359470.4:p.Gly312=
ENST00000422081.6:c.301G= ENSP00000477056.1:p.Gly101=
ENST00000441880.1:n.114-3288G=
ENST00000464251.5:c.860G= ENSP00000428980.1:n.860G=
ENST00000466323.5:c.*125G= ENSP00000418264.1:n.*125G=
ENST00000490775.5:n.719G=
NM_000202.6:c.934G= NP_000193.1:p.Gly312=
NM_001166550.2:c.664G= NP_001160022.1:p.Gly222=
NM_006123.4:c.934G= NP_006114.1:p.Gly312=
NR_104128.1:n.1281G=
NM_000202.7:c.934G= NP_000193.1:p.Gly312=
NM_001166550.3:c.664G= NP_001160022.1:p.Gly222=
NM_000202.8:c.934G= MANE Select NP_000193.1:p.Gly312=
NM_001166550.4:c.664G= NP_001160022.1:p.Gly222=
NM_006123.5:c.934G= NP_006114.1:p.Gly312=
NR_104128.2:n.1233G=