Canonical Allele Identifier: CA337035870

Gene: IDS

Linked Data

• dbSNP Id: rs994429617
• MyVariant Identifiers: chrX:g.149487229T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487229T>C , CM000685.2:g.149487229T>C	GRCh38
NC_000023.10:g.148568760T>C , CM000685.1:g.148568760T>C	GRCh37
NC_000023.9:g.148376665T>C	NCBI36
NG_011900.3:g.23106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-131A>G MANE Select	ENSP00000339801.6:n.1007-131A>G
ENST00000651111.1:c.374-131A>G	ENSP00000498395.1:n.374-131A>G
ENST00000340855.10:c.1007-131A>G	ENSP00000339801.6:n.1007-131A>G
ENST00000370441.8:c.*59A>G	ENSP00000359470.4:n.*59A>G
ENST00000422081.6:c.374-131A>G	ENSP00000477056.1:n.374-131A>G
ENST00000441880.1:n.114-131A>G
ENST00000466323.5:c.*282A>G	ENSP00000418264.1:n.*282A>G
ENST00000490775.5:n.876A>G
NM_000202.6:c.1007-131A>G	NP_000193.1:n.1007-131A>G
NM_001166550.2:c.737-131A>G	NP_001160022.1:n.737-131A>G
NM_006123.4:c.*59A>G	NP_006114.1:n.*59A>G
NR_104128.1:n.1438A>G
NM_000202.7:c.1007-131A>G	NP_000193.1:n.1007-131A>G
NM_001166550.3:c.737-131A>G	NP_001160022.1:n.737-131A>G
NM_000202.8:c.1007-131A>G MANE Select	NP_000193.1:n.1007-131A>G
NM_001166550.4:c.737-131A>G	NP_001160022.1:n.737-131A>G
NM_006123.5:c.*59A>G	NP_006114.1:n.*59A>G
NR_104128.2:n.1390A>G