Canonical Allele Identifier: CA519057751

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571979T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490448T>C , CM000685.2:g.149490448T>C	GRCh38
NC_000023.10:g.148571979T>C , CM000685.1:g.148571979T>C	GRCh37
NC_000023.9:g.148379884T>C	NCBI36
NG_011900.3:g.19887A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-8A>G MANE Select	ENSP00000339801.6:n.880-8A>G
ENST00000651111.1:c.247-8A>G	ENSP00000498395.1:n.247-8A>G
ENST00000340855.10:c.880-8A>G	ENSP00000339801.6:n.880-8A>G
ENST00000370441.8:c.880-8A>G	ENSP00000359470.4:n.880-8A>G
ENST00000422081.6:c.247-8A>G	ENSP00000477056.1:n.247-8A>G
ENST00000441880.1:n.114-3350A>G
ENST00000464251.5:c.806-8A>G	ENSP00000428980.1:n.806-8A>G
ENST00000466323.5:c.*71-8A>G	ENSP00000418264.1:n.*71-8A>G
ENST00000490775.5:n.665-8A>G
NM_000202.6:c.880-8A>G	NP_000193.1:n.880-8A>G
NM_001166550.2:c.610-8A>G	NP_001160022.1:n.610-8A>G
NM_006123.4:c.880-8A>G	NP_006114.1:n.880-8A>G
NR_104128.1:n.1227-8A>G
NM_000202.7:c.880-8A>G	NP_000193.1:n.880-8A>G
NM_001166550.3:c.610-8A>G	NP_001160022.1:n.610-8A>G
NM_000202.8:c.880-8A>G MANE Select	NP_000193.1:n.880-8A>G
NM_001166550.4:c.610-8A>G	NP_001160022.1:n.610-8A>G
NM_006123.5:c.880-8A>G	NP_006114.1:n.880-8A>G
NR_104128.2:n.1179-8A>G