Canonical Allele Identifier: CA414526156

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148584916T>G (hg19) ; chrX:g.149503386T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503386T>G , CM000685.2:g.149503386T>G	GRCh38
NC_000023.10:g.148584916T>G , CM000685.1:g.148584916T>G	GRCh37
NC_000023.9:g.148392821T>G	NCBI36
NG_011900.3:g.6949A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.344A>C MANE Select	ENSP00000339801.6:p.Asn115Thr
ENST00000651111.1:c.-215-2349A>C	ENSP00000498395.1:n.-215-2349A>C
ENST00000340855.10:c.344A>C	ENSP00000339801.6:p.Asn115Thr
ENST00000370441.8:c.344A>C	ENSP00000359470.4:p.Asn115Thr
ENST00000422081.6:c.-215-2349A>C	ENSP00000477056.1:n.-215-2349A>C
ENST00000427113.2:n.770-1163A>C
ENST00000428056.6:c.344A>C	ENSP00000390241.2:p.Asn115Thr
ENST00000441880.1:n.114-16288A>C
ENST00000464251.5:c.167A>C	ENSP00000428980.1:p.Asn56Thr
ENST00000466323.5:c.344A>C	ENSP00000418264.1:p.Asn115Thr
ENST00000490775.5:n.3A>C
ENST00000523759.5:n.533-2349A>C
NM_000202.6:c.344A>C	NP_000193.1:p.Asn115Thr
NM_001166550.2:c.74A>C	NP_001160022.1:p.Asn25Thr
NM_006123.4:c.344A>C	NP_006114.1:p.Asn115Thr
NR_104128.1:n.561A>C
NM_000202.7:c.344A>C	NP_000193.1:p.Asn115Thr
NM_001166550.3:c.74A>C	NP_001160022.1:p.Asn25Thr
NM_000202.8:c.344A>C MANE Select	NP_000193.1:p.Asn115Thr
NM_001166550.4:c.74A>C	NP_001160022.1:p.Asn25Thr
NM_006123.5:c.344A>C	NP_006114.1:p.Asn115Thr
NR_104128.2:n.513A>C