Canonical Allele Identifier: CA414522530

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579805T>G (hg19) ; chrX:g.149498274T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498274T>G , CM000685.2:g.149498274T>G	GRCh38
NC_000023.10:g.148579805T>G , CM000685.1:g.148579805T>G	GRCh37
NC_000023.9:g.148387710T>G	NCBI36
NG_011900.3:g.12061A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.541A>C MANE Select	ENSP00000339801.6:p.Asn181His
ENST00000651111.1:c.-93A>C	ENSP00000498395.1:n.-93A>C
ENST00000340855.10:c.541A>C	ENSP00000339801.6:p.Asn181His
ENST00000370441.8:c.541A>C	ENSP00000359470.4:p.Asn181His
ENST00000422081.6:c.-93A>C	ENSP00000477056.1:n.-93A>C
ENST00000441880.1:n.114-11176A>C
ENST00000464251.5:c.467A>C	ENSP00000428980.1:n.467A>C
ENST00000466323.5:c.541A>C	ENSP00000418264.1:p.Asn181His
ENST00000490775.5:n.326A>C
ENST00000523759.5:n.655A>C
NM_000202.6:c.541A>C	NP_000193.1:p.Asn181His
NM_001166550.2:c.271A>C	NP_001160022.1:p.Asn91His
NM_006123.4:c.541A>C	NP_006114.1:p.Asn181His
NR_104128.1:n.758A>C
NM_000202.7:c.541A>C	NP_000193.1:p.Asn181His
NM_001166550.3:c.271A>C	NP_001160022.1:p.Asn91His
NM_000202.8:c.541A>C MANE Select	NP_000193.1:p.Asn181His
NM_001166550.4:c.271A>C	NP_001160022.1:p.Asn91His
NM_006123.5:c.541A>C	NP_006114.1:p.Asn181His
NR_104128.2:n.710A>C