Canonical Allele Identifier: CA2695236562
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490313_149490314delinsAA , CM000685.2:g.149490313_149490314delinsAA GRCh38
NC_000023.10:g.148571844_148571845delinsAA , CM000685.1:g.148571844_148571845delinsAA GRCh37
NC_000023.9:g.148379749_148379750delinsAA NCBI36
NG_011900.3:g.20021_20022delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1006_1006+1delinsTT
ENST00000651111.1:c.373_373+1delinsTT
ENST00000340855.10:c.1006_1006+1delinsTT
ENST00000370441.8:c.1006_1006+1delinsTT
ENST00000422081.6:c.373_373+1delinsTT
ENST00000441880.1:n.114-3216_114-3215delinsTT
ENST00000464251.5:c.932_932+1delinsTT
ENST00000466323.5:c.*197_*197+1delinsTT
ENST00000490775.5:n.791_791+1delinsTT
NM_000202.6:c.1006_1006+1delinsTT
NM_001166550.2:c.736_736+1delinsTT
NM_006123.4:c.1006_1006+1delinsTT
NR_104128.1:n.1353_1353+1delinsTT
NM_000202.7:c.1006_1006+1delinsTT
NM_001166550.3:c.736_736+1delinsTT
NM_000202.8:c.1006_1006+1delinsTT
NM_001166550.4:c.736_736+1delinsTT
NM_006123.5:c.1006_1006+1delinsTT
NR_104128.2:n.1305_1305+1delinsTT