Canonical Allele Identifier: CA2465010061
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149500911G= , CM000685.2:g.149500911G= GRCh38
NC_000023.10:g.148582442G= , CM000685.1:g.148582442G= GRCh37
NC_000023.9:g.148390347G= NCBI36
NG_011900.3:g.9424C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.507+38C= MANE Select ENSP00000339801.6:n.507+38C=
ENST00000651111.1:c.-127+38C= ENSP00000498395.1:n.-127+38C=
ENST00000340855.10:c.507+38C= ENSP00000339801.6:n.507+38C=
ENST00000370441.8:c.507+38C= ENSP00000359470.4:n.507+38C=
ENST00000422081.6:c.-127+38C= ENSP00000477056.1:n.-127+38C=
ENST00000441880.1:n.114-13813C=
ENST00000464251.5:c.433+38C= ENSP00000428980.1:n.433+38C=
ENST00000466323.5:c.507+38C= ENSP00000418264.1:n.507+38C=
ENST00000490775.5:n.166+38C=
ENST00000523759.5:n.621+38C=
NM_000202.6:c.507+38C= NP_000193.1:n.507+38C=
NM_001166550.2:c.237+38C= NP_001160022.1:n.237+38C=
NM_006123.4:c.507+38C= NP_006114.1:n.507+38C=
NR_104128.1:n.724+38C=
NM_000202.7:c.507+38C= NP_000193.1:n.507+38C=
NM_001166550.3:c.237+38C= NP_001160022.1:n.237+38C=
NM_000202.8:c.507+38C= MANE Select NP_000193.1:n.507+38C=
NM_001166550.4:c.237+38C= NP_001160022.1:n.237+38C=
NM_006123.5:c.507+38C= NP_006114.1:n.507+38C=
NR_104128.2:n.676+38C=