Canonical Allele Identifier: CA2602434066

Gene: IDS

Linked Data

• dbSNP Id: rs2124042602
• gnomAD v3: X-149496684-A-G
• gnomAD v4: X-149496684-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496684A>G , CM000685.2:g.149496684A>G	GRCh38
NC_000023.10:g.148578215A>G , CM000685.1:g.148578215A>G	GRCh37
NC_000023.9:g.148386120A>G	NCBI36
NG_011900.3:g.13651T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-168T>C MANE Select	ENSP00000339801.6:n.709-168T>C
ENST00000651111.1:c.76-168T>C	ENSP00000498395.1:n.76-168T>C
ENST00000340855.10:c.709-168T>C	ENSP00000339801.6:n.709-168T>C
ENST00000370441.8:c.709-168T>C	ENSP00000359470.4:n.709-168T>C
ENST00000422081.6:c.76-168T>C	ENSP00000477056.1:n.76-168T>C
ENST00000441880.1:n.114-9586T>C
ENST00000464251.5:c.635-168T>C	ENSP00000428980.1:n.635-168T>C
ENST00000466019.1:n.161-168T>C
ENST00000466323.5:c.709-168T>C	ENSP00000418264.1:n.709-168T>C
ENST00000490775.5:n.494-168T>C
NM_000202.6:c.709-168T>C	NP_000193.1:n.709-168T>C
NM_001166550.2:c.439-168T>C	NP_001160022.1:n.439-168T>C
NM_006123.4:c.709-168T>C	NP_006114.1:n.709-168T>C
NR_104128.1:n.926-168T>C
NM_000202.7:c.709-168T>C	NP_000193.1:n.709-168T>C
NM_001166550.3:c.439-168T>C	NP_001160022.1:n.439-168T>C
NM_000202.8:c.709-168T>C MANE Select	NP_000193.1:n.709-168T>C
NM_001166550.4:c.439-168T>C	NP_001160022.1:n.439-168T>C
NM_006123.5:c.709-168T>C	NP_006114.1:n.709-168T>C
NR_104128.2:n.878-168T>C