Canonical Allele Identifier: CA414519925

Gene: IDS

Linked Data

• gnomAD v4: X-149490334-A-G
• MyVariant Identifiers: chrX:g.148571865A>G (hg19) ; chrX:g.149490334A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490334A>G , CM000685.2:g.149490334A>G	GRCh38
NC_000023.10:g.148571865A>G , CM000685.1:g.148571865A>G	GRCh37
NC_000023.9:g.148379770A>G	NCBI36
NG_011900.3:g.20001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.986T>C MANE Select	ENSP00000339801.6:p.Ile329Thr
ENST00000651111.1:c.353T>C	ENSP00000498395.1:p.Ile118Thr
ENST00000340855.10:c.986T>C	ENSP00000339801.6:p.Ile329Thr
ENST00000370441.8:c.986T>C	ENSP00000359470.4:p.Ile329Thr
ENST00000422081.6:c.353T>C	ENSP00000477056.1:p.Ile118Thr
ENST00000441880.1:n.114-3236T>C
ENST00000464251.5:c.912T>C	ENSP00000428980.1:n.912T>C
ENST00000466323.5:c.*177T>C	ENSP00000418264.1:n.*177T>C
ENST00000490775.5:n.771T>C
NM_000202.6:c.986T>C	NP_000193.1:p.Ile329Thr
NM_001166550.2:c.716T>C	NP_001160022.1:p.Ile239Thr
NM_006123.4:c.986T>C	NP_006114.1:p.Ile329Thr
NR_104128.1:n.1333T>C
NM_000202.7:c.986T>C	NP_000193.1:p.Ile329Thr
NM_001166550.3:c.716T>C	NP_001160022.1:p.Ile239Thr
NM_000202.8:c.986T>C MANE Select	NP_000193.1:p.Ile329Thr
NM_001166550.4:c.716T>C	NP_001160022.1:p.Ile239Thr
NM_006123.5:c.986T>C	NP_006114.1:p.Ile329Thr
NR_104128.2:n.1285T>C