Canonical Allele Identifier: CA414522295

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579714T>C (hg19) ; chrX:g.149498183T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498183T>C , CM000685.2:g.149498183T>C	GRCh38
NC_000023.10:g.148579714T>C , CM000685.1:g.148579714T>C	GRCh37
NC_000023.9:g.148387619T>C	NCBI36
NG_011900.3:g.12152A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.632A>G MANE Select	ENSP00000339801.6:p.Lys211Arg
ENST00000651111.1:c.-2A>G	ENSP00000498395.1:n.-2A>G
ENST00000340855.10:c.632A>G	ENSP00000339801.6:p.Lys211Arg
ENST00000370441.8:c.632A>G	ENSP00000359470.4:p.Lys211Arg
ENST00000422081.6:c.-2A>G	ENSP00000477056.1:n.-2A>G
ENST00000441880.1:n.114-11085A>G
ENST00000464251.5:c.558A>G	ENSP00000428980.1:n.558A>G
ENST00000466019.1:n.84A>G
ENST00000466323.5:c.632A>G	ENSP00000418264.1:p.Lys211Arg
ENST00000490775.5:n.417A>G
NM_000202.6:c.632A>G	NP_000193.1:p.Lys211Arg
NM_001166550.2:c.362A>G	NP_001160022.1:p.Lys121Arg
NM_006123.4:c.632A>G	NP_006114.1:p.Lys211Arg
NR_104128.1:n.849A>G
NM_000202.7:c.632A>G	NP_000193.1:p.Lys211Arg
NM_001166550.3:c.362A>G	NP_001160022.1:p.Lys121Arg
NM_000202.8:c.632A>G MANE Select	NP_000193.1:p.Lys211Arg
NM_001166550.4:c.362A>G	NP_001160022.1:p.Lys121Arg
NM_006123.5:c.632A>G	NP_006114.1:p.Lys211Arg
NR_104128.2:n.801A>G