Canonical Allele Identifier: CA519058329

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579713C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498182C>T , CM000685.2:g.149498182C>T	GRCh38
NC_000023.10:g.148579713C>T , CM000685.1:g.148579713C>T	GRCh37
NC_000023.9:g.148387618C>T	NCBI36
NG_011900.3:g.12153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.633G>A MANE Select	ENSP00000339801.6:p.Lys211=
ENST00000651111.1:c.-1G>A	ENSP00000498395.1:n.-1G>A
ENST00000340855.10:c.633G>A	ENSP00000339801.6:p.Lys211=
ENST00000370441.8:c.633G>A	ENSP00000359470.4:p.Lys211=
ENST00000422081.6:c.-1G>A	ENSP00000477056.1:n.-1G>A
ENST00000441880.1:n.114-11084G>A
ENST00000464251.5:c.559G>A	ENSP00000428980.1:n.559G>A
ENST00000466019.1:n.85G>A
ENST00000466323.5:c.633G>A	ENSP00000418264.1:p.Lys211=
ENST00000490775.5:n.418G>A
NM_000202.6:c.633G>A	NP_000193.1:p.Lys211=
NM_001166550.2:c.363G>A	NP_001160022.1:p.Lys121=
NM_006123.4:c.633G>A	NP_006114.1:p.Lys211=
NR_104128.1:n.850G>A
NM_000202.7:c.633G>A	NP_000193.1:p.Lys211=
NM_001166550.3:c.363G>A	NP_001160022.1:p.Lys121=
NM_000202.8:c.633G>A MANE Select	NP_000193.1:p.Lys211=
NM_001166550.4:c.363G>A	NP_001160022.1:p.Lys121=
NM_006123.5:c.633G>A	NP_006114.1:p.Lys211=
NR_104128.2:n.802G>A