Canonical Allele Identifier: CA414522132

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579642G>T (hg19) ; chrX:g.149498111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498111G>T , CM000685.2:g.149498111G>T	GRCh38
NC_000023.10:g.148579642G>T , CM000685.1:g.148579642G>T	GRCh37
NC_000023.9:g.148387547G>T	NCBI36
NG_011900.3:g.12224C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.704C>A MANE Select	ENSP00000339801.6:p.Pro235His
ENST00000651111.1:c.71C>A	ENSP00000498395.1:p.Pro24His
ENST00000340855.10:c.704C>A	ENSP00000339801.6:p.Pro235His
ENST00000370441.8:c.704C>A	ENSP00000359470.4:p.Pro235His
ENST00000422081.6:c.71C>A	ENSP00000477056.1:p.Pro24His
ENST00000441880.1:n.114-11013C>A
ENST00000464251.5:c.630C>A	ENSP00000428980.1:n.630C>A
ENST00000466019.1:n.156C>A
ENST00000466323.5:c.704C>A	ENSP00000418264.1:p.Pro235His
ENST00000490775.5:n.489C>A
NM_000202.6:c.704C>A	NP_000193.1:p.Pro235His
NM_001166550.2:c.434C>A	NP_001160022.1:p.Pro145His
NM_006123.4:c.704C>A	NP_006114.1:p.Pro235His
NR_104128.1:n.921C>A
NM_000202.7:c.704C>A	NP_000193.1:p.Pro235His
NM_001166550.3:c.434C>A	NP_001160022.1:p.Pro145His
NM_000202.8:c.704C>A MANE Select	NP_000193.1:p.Pro235His
NM_001166550.4:c.434C>A	NP_001160022.1:p.Pro145His
NM_006123.5:c.704C>A	NP_006114.1:p.Pro235His
NR_104128.2:n.873C>A