Canonical Allele Identifier: CA414526044

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148584902G>C (hg19) ; chrX:g.149503372G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503372G>C , CM000685.2:g.149503372G>C	GRCh38
NC_000023.10:g.148584902G>C , CM000685.1:g.148584902G>C	GRCh37
NC_000023.9:g.148392807G>C	NCBI36
NG_011900.3:g.6963C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.358C>G MANE Select	ENSP00000339801.6:p.Pro120Ala
ENST00000651111.1:c.-215-2335C>G	ENSP00000498395.1:n.-215-2335C>G
ENST00000340855.10:c.358C>G	ENSP00000339801.6:p.Pro120Ala
ENST00000370441.8:c.358C>G	ENSP00000359470.4:p.Pro120Ala
ENST00000422081.6:c.-215-2335C>G	ENSP00000477056.1:n.-215-2335C>G
ENST00000427113.2:n.770-1149C>G
ENST00000428056.6:c.358C>G	ENSP00000390241.2:p.Pro120Ala
ENST00000441880.1:n.114-16274C>G
ENST00000464251.5:c.181C>G	ENSP00000428980.1:p.Pro61Ala
ENST00000466323.5:c.358C>G	ENSP00000418264.1:p.Pro120Ala
ENST00000490775.5:n.17C>G
ENST00000523759.5:n.533-2335C>G
NM_000202.6:c.358C>G	NP_000193.1:p.Pro120Ala
NM_001166550.2:c.88C>G	NP_001160022.1:p.Pro30Ala
NM_006123.4:c.358C>G	NP_006114.1:p.Pro120Ala
NR_104128.1:n.575C>G
NM_000202.7:c.358C>G	NP_000193.1:p.Pro120Ala
NM_001166550.3:c.88C>G	NP_001160022.1:p.Pro30Ala
NM_000202.8:c.358C>G MANE Select	NP_000193.1:p.Pro120Ala
NM_001166550.4:c.88C>G	NP_001160022.1:p.Pro30Ala
NM_006123.5:c.358C>G	NP_006114.1:p.Pro120Ala
NR_104128.2:n.527C>G