Canonical Allele Identifier: CA414522191

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579667T>C (hg19) ; chrX:g.149498136T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498136T>C , CM000685.2:g.149498136T>C	GRCh38
NC_000023.10:g.148579667T>C , CM000685.1:g.148579667T>C	GRCh37
NC_000023.9:g.148387572T>C	NCBI36
NG_011900.3:g.12199A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.679A>G MANE Select	ENSP00000339801.6:p.Lys227Glu
ENST00000651111.1:c.46A>G	ENSP00000498395.1:p.Lys16Glu
ENST00000340855.10:c.679A>G	ENSP00000339801.6:p.Lys227Glu
ENST00000370441.8:c.679A>G	ENSP00000359470.4:p.Lys227Glu
ENST00000422081.6:c.46A>G	ENSP00000477056.1:p.Lys16Glu
ENST00000441880.1:n.114-11038A>G
ENST00000464251.5:c.605A>G	ENSP00000428980.1:n.605A>G
ENST00000466019.1:n.131A>G
ENST00000466323.5:c.679A>G	ENSP00000418264.1:p.Lys227Glu
ENST00000490775.5:n.464A>G
NM_000202.6:c.679A>G	NP_000193.1:p.Lys227Glu
NM_001166550.2:c.409A>G	NP_001160022.1:p.Lys137Glu
NM_006123.4:c.679A>G	NP_006114.1:p.Lys227Glu
NR_104128.1:n.896A>G
NM_000202.7:c.679A>G	NP_000193.1:p.Lys227Glu
NM_001166550.3:c.409A>G	NP_001160022.1:p.Lys137Glu
NM_000202.8:c.679A>G MANE Select	NP_000193.1:p.Lys227Glu
NM_001166550.4:c.409A>G	NP_001160022.1:p.Lys137Glu
NM_006123.5:c.679A>G	NP_006114.1:p.Lys227Glu
NR_104128.2:n.848A>G