Canonical Allele Identifier: CA519060899

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148584900G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503370G>A , CM000685.2:g.149503370G>A	GRCh38
NC_000023.10:g.148584900G>A , CM000685.1:g.148584900G>A	GRCh37
NC_000023.9:g.148392805G>A	NCBI36
NG_011900.3:g.6965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.360C>T MANE Select	ENSP00000339801.6:p.Pro120=
ENST00000651111.1:c.-215-2333C>T	ENSP00000498395.1:n.-215-2333C>T
ENST00000340855.10:c.360C>T	ENSP00000339801.6:p.Pro120=
ENST00000370441.8:c.360C>T	ENSP00000359470.4:p.Pro120=
ENST00000422081.6:c.-215-2333C>T	ENSP00000477056.1:n.-215-2333C>T
ENST00000427113.2:n.770-1147C>T
ENST00000428056.6:c.360C>T	ENSP00000390241.2:p.Pro120=
ENST00000441880.1:n.114-16272C>T
ENST00000464251.5:c.183C>T	ENSP00000428980.1:p.Pro61=
ENST00000466323.5:c.360C>T	ENSP00000418264.1:p.Pro120=
ENST00000490775.5:n.19C>T
ENST00000523759.5:n.533-2333C>T
NM_000202.6:c.360C>T	NP_000193.1:p.Pro120=
NM_001166550.2:c.90C>T	NP_001160022.1:p.Pro30=
NM_006123.4:c.360C>T	NP_006114.1:p.Pro120=
NR_104128.1:n.577C>T
NM_000202.7:c.360C>T	NP_000193.1:p.Pro120=
NM_001166550.3:c.90C>T	NP_001160022.1:p.Pro30=
NM_000202.8:c.360C>T MANE Select	NP_000193.1:p.Pro120=
NM_001166550.4:c.90C>T	NP_001160022.1:p.Pro30=
NM_006123.5:c.360C>T	NP_006114.1:p.Pro120=
NR_104128.2:n.529C>T