Canonical Allele Identifier: CA414522196

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579669T>G (hg19) ; chrX:g.149498138T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498138T>G , CM000685.2:g.149498138T>G	GRCh38
NC_000023.10:g.148579669T>G , CM000685.1:g.148579669T>G	GRCh37
NC_000023.9:g.148387574T>G	NCBI36
NG_011900.3:g.12197A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.677A>C MANE Select	ENSP00000339801.6:p.His226Pro
ENST00000651111.1:c.44A>C	ENSP00000498395.1:p.His15Pro
ENST00000340855.10:c.677A>C	ENSP00000339801.6:p.His226Pro
ENST00000370441.8:c.677A>C	ENSP00000359470.4:p.His226Pro
ENST00000422081.6:c.44A>C	ENSP00000477056.1:p.His15Pro
ENST00000441880.1:n.114-11040A>C
ENST00000464251.5:c.603A>C	ENSP00000428980.1:n.603A>C
ENST00000466019.1:n.129A>C
ENST00000466323.5:c.677A>C	ENSP00000418264.1:p.His226Pro
ENST00000490775.5:n.462A>C
NM_000202.6:c.677A>C	NP_000193.1:p.His226Pro
NM_001166550.2:c.407A>C	NP_001160022.1:p.His136Pro
NM_006123.4:c.677A>C	NP_006114.1:p.His226Pro
NR_104128.1:n.894A>C
NM_000202.7:c.677A>C	NP_000193.1:p.His226Pro
NM_001166550.3:c.407A>C	NP_001160022.1:p.His136Pro
NM_000202.8:c.677A>C MANE Select	NP_000193.1:p.His226Pro
NM_001166550.4:c.407A>C	NP_001160022.1:p.His136Pro
NM_006123.5:c.677A>C	NP_006114.1:p.His226Pro
NR_104128.2:n.846A>C