Canonical Allele Identifier: CA2465010062
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149500912_149500913delinsTG , CM000685.2:g.149500912_149500913delinsTG GRCh38
NC_000023.10:g.148582443_148582444delinsTG , CM000685.1:g.148582443_148582444delinsTG GRCh37
NC_000023.9:g.148390348_148390349delinsTG NCBI36
NG_011900.3:g.9422_9423delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.507+36_507+37delinsCA MANE Select ENSP00000339801.6:n.507+36_507+37delinsCA...
ENST00000651111.1:c.-127+36_-127+37delinsCA ENSP00000498395.1:n.-127+36_-127+37delins...
ENST00000340855.10:c.507+36_507+37delinsCA ENSP00000339801.6:n.507+36_507+37delinsCA...
ENST00000370441.8:c.507+36_507+37delinsCA ENSP00000359470.4:n.507+36_507+37delinsCA...
ENST00000422081.6:c.-127+36_-127+37delinsCA ENSP00000477056.1:n.-127+36_-127+37delins...
ENST00000441880.1:n.114-13815_114-13814delinsCA
ENST00000464251.5:c.433+36_433+37delinsCA ENSP00000428980.1:n.433+36_433+37delinsCA...
ENST00000466323.5:c.507+36_507+37delinsCA ENSP00000418264.1:n.507+36_507+37delinsCA...
ENST00000490775.5:n.166+36_166+37delinsCA
ENST00000523759.5:n.621+36_621+37delinsCA
NM_000202.6:c.507+36_507+37delinsCA NP_000193.1:n.507+36_507+37delinsCA
NM_001166550.2:c.237+36_237+37delinsCA NP_001160022.1:n.237+36_237+37delinsCA
NM_006123.4:c.507+36_507+37delinsCA NP_006114.1:n.507+36_507+37delinsCA
NR_104128.1:n.724+36_724+37delinsCA
NM_000202.7:c.507+36_507+37delinsCA NP_000193.1:n.507+36_507+37delinsCA
NM_001166550.3:c.237+36_237+37delinsCA NP_001160022.1:n.237+36_237+37delinsCA
NM_000202.8:c.507+36_507+37delinsCA MANE Select NP_000193.1:n.507+36_507+37delinsCA
NM_001166550.4:c.237+36_237+37delinsCA NP_001160022.1:n.237+36_237+37delinsCA
NM_006123.5:c.507+36_507+37delinsCA NP_006114.1:n.507+36_507+37delinsCA
NR_104128.2:n.676+36_676+37delinsCA