Canonical Allele Identifier: CA2465009230
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498205G= , CM000685.2:g.149498205G= GRCh38
NC_000023.10:g.148579736G= , CM000685.1:g.148579736G= GRCh37
NC_000023.9:g.148387641G= NCBI36
NG_011900.3:g.12130C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.610C= MANE Select ENSP00000339801.6:p.Gln204=
ENST00000651111.1:c.-24C= ENSP00000498395.1:n.-24C=
ENST00000340855.10:c.610C= ENSP00000339801.6:p.Gln204=
ENST00000370441.8:c.610C= ENSP00000359470.4:p.Gln204=
ENST00000422081.6:c.-24C= ENSP00000477056.1:n.-24C=
ENST00000441880.1:n.114-11107C=
ENST00000464251.5:c.536C= ENSP00000428980.1:n.536C=
ENST00000466019.1:n.62C=
ENST00000466323.5:c.610C= ENSP00000418264.1:p.Gln204=
ENST00000490775.5:n.395C=
ENST00000523759.5:n.724C=
NM_000202.6:c.610C= NP_000193.1:p.Gln204=
NM_001166550.2:c.340C= NP_001160022.1:p.Gln114=
NM_006123.4:c.610C= NP_006114.1:p.Gln204=
NR_104128.1:n.827C=
NM_000202.7:c.610C= NP_000193.1:p.Gln204=
NM_001166550.3:c.340C= NP_001160022.1:p.Gln114=
NM_000202.8:c.610C= MANE Select NP_000193.1:p.Gln204=
NM_001166550.4:c.340C= NP_001160022.1:p.Gln114=
NM_006123.5:c.610C= NP_006114.1:p.Gln204=
NR_104128.2:n.779C=