Canonical Allele Identifier: CA414522111

Gene: IDS

Linked Data

• COSMIC: COSM1466256 ; COSM4783903 ; COSM4783904
• MyVariant Identifiers: chrX:g.148578048C>A (hg19) ; chrX:g.149496517C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496517C>A , CM000685.2:g.149496517C>A	GRCh38
NC_000023.10:g.148578048C>A , CM000685.1:g.148578048C>A	GRCh37
NC_000023.9:g.148385953C>A	NCBI36
NG_011900.3:g.13818G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-1G>T MANE Select	ENSP00000339801.6:n.709-1G>T
ENST00000651111.1:c.76-1G>T	ENSP00000498395.1:n.76-1G>T
ENST00000340855.10:c.709-1G>T	ENSP00000339801.6:n.709-1G>T
ENST00000370441.8:c.709-1G>T	ENSP00000359470.4:n.709-1G>T
ENST00000422081.6:c.76-1G>T	ENSP00000477056.1:n.76-1G>T
ENST00000441880.1:n.114-9419G>T
ENST00000464251.5:c.635-1G>T	ENSP00000428980.1:n.635-1G>T
ENST00000466019.1:n.161-1G>T
ENST00000466323.5:c.709-1G>T	ENSP00000418264.1:n.709-1G>T
ENST00000490775.5:n.494-1G>T
NM_000202.6:c.709-1G>T	NP_000193.1:n.709-1G>T
NM_001166550.2:c.439-1G>T	NP_001160022.1:n.439-1G>T
NM_006123.4:c.709-1G>T	NP_006114.1:n.709-1G>T
NR_104128.1:n.926-1G>T
NM_000202.7:c.709-1G>T	NP_000193.1:n.709-1G>T
NM_001166550.3:c.439-1G>T	NP_001160022.1:n.439-1G>T
NM_000202.8:c.709-1G>T MANE Select	NP_000193.1:n.709-1G>T
NM_001166550.4:c.439-1G>T	NP_001160022.1:n.439-1G>T
NM_006123.5:c.709-1G>T	NP_006114.1:n.709-1G>T
NR_104128.2:n.878-1G>T