Canonical Allele Identifier: CA414522421

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579754C>G (hg19) ; chrX:g.149498223C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498223C>G , CM000685.2:g.149498223C>G	GRCh38
NC_000023.10:g.148579754C>G , CM000685.1:g.148579754C>G	GRCh37
NC_000023.9:g.148387659C>G	NCBI36
NG_011900.3:g.12112G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.592G>C MANE Select	ENSP00000339801.6:p.Asp198His
ENST00000651111.1:c.-42G>C	ENSP00000498395.1:n.-42G>C
ENST00000340855.10:c.592G>C	ENSP00000339801.6:p.Asp198His
ENST00000370441.8:c.592G>C	ENSP00000359470.4:p.Asp198His
ENST00000422081.6:c.-42G>C	ENSP00000477056.1:n.-42G>C
ENST00000441880.1:n.114-11125G>C
ENST00000464251.5:c.518G>C	ENSP00000428980.1:n.518G>C
ENST00000466019.1:n.44G>C
ENST00000466323.5:c.592G>C	ENSP00000418264.1:p.Asp198His
ENST00000490775.5:n.377G>C
ENST00000523759.5:n.706G>C
NM_000202.6:c.592G>C	NP_000193.1:p.Asp198His
NM_001166550.2:c.322G>C	NP_001160022.1:p.Asp108His
NM_006123.4:c.592G>C	NP_006114.1:p.Asp198His
NR_104128.1:n.809G>C
NM_000202.7:c.592G>C	NP_000193.1:p.Asp198His
NM_001166550.3:c.322G>C	NP_001160022.1:p.Asp108His
NM_000202.8:c.592G>C MANE Select	NP_000193.1:p.Asp198His
NM_001166550.4:c.322G>C	NP_001160022.1:p.Asp108His
NM_006123.5:c.592G>C	NP_006114.1:p.Asp198His
NR_104128.2:n.761G>C