Canonical Allele Identifier: CA2465005649

Gene: IDS

Linked Data

• dbSNP Id: rs2089344685

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487199G>A , CM000685.2:g.149487199G>A	GRCh38
NC_000023.10:g.148568730G>A , CM000685.1:g.148568730G>A	GRCh37
NC_000023.9:g.148376635G>A	NCBI36
NG_011900.3:g.23136C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-101C>T MANE Select	ENSP00000339801.6:n.1007-101C>T
ENST00000651111.1:c.374-101C>T	ENSP00000498395.1:n.374-101C>T
ENST00000340855.10:c.1007-101C>T	ENSP00000339801.6:n.1007-101C>T
ENST00000370441.8:c.*89C>T	ENSP00000359470.4:n.*89C>T
ENST00000422081.6:c.374-101C>T	ENSP00000477056.1:n.374-101C>T
ENST00000441880.1:n.114-101C>T
ENST00000466323.5:c.*312C>T	ENSP00000418264.1:n.*312C>T
ENST00000490775.5:n.906C>T
NM_000202.6:c.1007-101C>T	NP_000193.1:n.1007-101C>T
NM_001166550.2:c.737-101C>T	NP_001160022.1:n.737-101C>T
NM_006123.4:c.*89C>T	NP_006114.1:n.*89C>T
NR_104128.1:n.1468C>T
NM_000202.7:c.1007-101C>T	NP_000193.1:n.1007-101C>T
NM_001166550.3:c.737-101C>T	NP_001160022.1:n.737-101C>T
NM_000202.8:c.1007-101C>T MANE Select	NP_000193.1:n.1007-101C>T
NM_001166550.4:c.737-101C>T	NP_001160022.1:n.737-101C>T
NM_006123.5:c.*89C>T	NP_006114.1:n.*89C>T
NR_104128.2:n.1420C>T