Canonical Allele Identifier: CA414520044

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571885C>A (hg19) ; chrX:g.149490354C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490354C>A , CM000685.2:g.149490354C>A	GRCh38
NC_000023.10:g.148571885C>A , CM000685.1:g.148571885C>A	GRCh37
NC_000023.9:g.148379790C>A	NCBI36
NG_011900.3:g.19981G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.966G>T MANE Select	ENSP00000339801.6:p.Gln322His
ENST00000651111.1:c.333G>T	ENSP00000498395.1:p.Gln111His
ENST00000340855.10:c.966G>T	ENSP00000339801.6:p.Gln322His
ENST00000370441.8:c.966G>T	ENSP00000359470.4:p.Gln322His
ENST00000422081.6:c.333G>T	ENSP00000477056.1:p.Gln111His
ENST00000441880.1:n.114-3256G>T
ENST00000464251.5:c.892G>T	ENSP00000428980.1:n.892G>T
ENST00000466323.5:c.*157G>T	ENSP00000418264.1:n.*157G>T
ENST00000490775.5:n.751G>T
NM_000202.6:c.966G>T	NP_000193.1:p.Gln322His
NM_001166550.2:c.696G>T	NP_001160022.1:p.Gln232His
NM_006123.4:c.966G>T	NP_006114.1:p.Gln322His
NR_104128.1:n.1313G>T
NM_000202.7:c.966G>T	NP_000193.1:p.Gln322His
NM_001166550.3:c.696G>T	NP_001160022.1:p.Gln232His
NM_000202.8:c.966G>T MANE Select	NP_000193.1:p.Gln322His
NM_001166550.4:c.696G>T	NP_001160022.1:p.Gln232His
NM_006123.5:c.966G>T	NP_006114.1:p.Gln322His
NR_104128.2:n.1265G>T