Canonical Allele Identifier: CA414522130

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579640T>A (hg19) ; chrX:g.149498109T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498109T>A , CM000685.2:g.149498109T>A	GRCh38
NC_000023.10:g.148579640T>A , CM000685.1:g.148579640T>A	GRCh37
NC_000023.9:g.148387545T>A	NCBI36
NG_011900.3:g.12226A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.706A>T MANE Select	ENSP00000339801.6:p.Lys236Ter
ENST00000651111.1:c.73A>T	ENSP00000498395.1:p.Lys25Ter
ENST00000340855.10:c.706A>T	ENSP00000339801.6:p.Lys236Ter
ENST00000370441.8:c.706A>T	ENSP00000359470.4:p.Lys236Ter
ENST00000422081.6:c.73A>T	ENSP00000477056.1:p.Lys25Ter
ENST00000441880.1:n.114-11011A>T
ENST00000464251.5:c.632A>T	ENSP00000428980.1:n.632A>T
ENST00000466019.1:n.158A>T
ENST00000466323.5:c.706A>T	ENSP00000418264.1:p.Lys236Ter
ENST00000490775.5:n.491A>T
NM_000202.6:c.706A>T	NP_000193.1:p.Lys236Ter
NM_001166550.2:c.436A>T	NP_001160022.1:p.Lys146Ter
NM_006123.4:c.706A>T	NP_006114.1:p.Lys236Ter
NR_104128.1:n.923A>T
NM_000202.7:c.706A>T	NP_000193.1:p.Lys236Ter
NM_001166550.3:c.436A>T	NP_001160022.1:p.Lys146Ter
NM_000202.8:c.706A>T MANE Select	NP_000193.1:p.Lys236Ter
NM_001166550.4:c.436A>T	NP_001160022.1:p.Lys146Ter
NM_006123.5:c.706A>T	NP_006114.1:p.Lys236Ter
NR_104128.2:n.875A>T