Canonical Allele Identifier: CA2694897996

Gene: IDS

Linked Data

• gnomAD v4: X-149496328-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496328A>C , CM000685.2:g.149496328A>C	GRCh38
NC_000023.10:g.148577859A>C , CM000685.1:g.148577859A>C	GRCh37
NC_000023.9:g.148385764A>C	NCBI36
NG_011900.3:g.14007T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.879+18T>G MANE Select	ENSP00000339801.6:n.879+18T>G
ENST00000651111.1:c.246+18T>G	ENSP00000498395.1:n.246+18T>G
ENST00000340855.10:c.879+18T>G	ENSP00000339801.6:n.879+18T>G
ENST00000370441.8:c.879+18T>G	ENSP00000359470.4:n.879+18T>G
ENST00000422081.6:c.246+18T>G	ENSP00000477056.1:n.246+18T>G
ENST00000441880.1:n.114-9230T>G
ENST00000464251.5:c.805+18T>G	ENSP00000428980.1:n.805+18T>G
ENST00000466019.1:n.331+18T>G
ENST00000466323.5:c.879+18T>G	ENSP00000418264.1:n.879+18T>G
ENST00000490775.5:n.664+18T>G
NM_000202.6:c.879+18T>G	NP_000193.1:n.879+18T>G
NM_001166550.2:c.609+18T>G	NP_001160022.1:n.609+18T>G
NM_006123.4:c.879+18T>G	NP_006114.1:n.879+18T>G
NR_104128.1:n.1096+18T>G
NM_000202.7:c.879+18T>G	NP_000193.1:n.879+18T>G
NM_001166550.3:c.609+18T>G	NP_001160022.1:n.609+18T>G
NM_000202.8:c.879+18T>G MANE Select	NP_000193.1:n.879+18T>G
NM_001166550.4:c.609+18T>G	NP_001160022.1:n.609+18T>G
NM_006123.5:c.879+18T>G	NP_006114.1:n.879+18T>G
NR_104128.2:n.1048+18T>G