Canonical Allele Identifier: CA2465006763
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490317G= , CM000685.2:g.149490317G= GRCh38
NC_000023.10:g.148571848G= , CM000685.1:g.148571848G= GRCh37
NC_000023.9:g.148379753G= NCBI36
NG_011900.3:g.20018C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1003C= MANE Select ENSP00000339801.6:p.His335=
ENST00000651111.1:c.370C= ENSP00000498395.1:p.His124=
ENST00000340855.10:c.1003C= ENSP00000339801.6:p.His335=
ENST00000370441.8:c.1003C= ENSP00000359470.4:p.His335=
ENST00000422081.6:c.370C= ENSP00000477056.1:p.His124=
ENST00000441880.1:n.114-3219C=
ENST00000464251.5:c.929C= ENSP00000428980.1:n.929C=
ENST00000466323.5:c.*194C= ENSP00000418264.1:n.*194C=
ENST00000490775.5:n.788C=
NM_000202.6:c.1003C= NP_000193.1:p.His335=
NM_001166550.2:c.733C= NP_001160022.1:p.His245=
NM_006123.4:c.1003C= NP_006114.1:p.His335=
NR_104128.1:n.1350C=
NM_000202.7:c.1003C= NP_000193.1:p.His335=
NM_001166550.3:c.733C= NP_001160022.1:p.His245=
NM_000202.8:c.1003C= MANE Select NP_000193.1:p.His335=
NM_001166550.4:c.733C= NP_001160022.1:p.His245=
NM_006123.5:c.1003C= NP_006114.1:p.His335=
NR_104128.2:n.1302C=