Canonical Allele Identifier: CA645069001

Gene: IDS

Linked Data

• dbSNP Id: rs1464050026
• gnomAD v2: X-148572385-T-G
• gnomAD v3: X-149490854-T-G
• gnomAD v4: X-149490854-T-G
• MyVariant Identifiers: chrX:g.148572385T>G (hg19) ; chrX:g.149490854T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490854T>G , CM000685.2:g.149490854T>G	GRCh38
NC_000023.10:g.148572385T>G , CM000685.1:g.148572385T>G	GRCh37
NC_000023.9:g.148380290T>G	NCBI36
NG_011900.3:g.19481A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-414A>C MANE Select	ENSP00000339801.6:n.880-414A>C
ENST00000651111.1:c.247-414A>C	ENSP00000498395.1:n.247-414A>C
ENST00000340855.10:c.880-414A>C	ENSP00000339801.6:n.880-414A>C
ENST00000370441.8:c.880-414A>C	ENSP00000359470.4:n.880-414A>C
ENST00000422081.6:c.247-414A>C	ENSP00000477056.1:n.247-414A>C
ENST00000441880.1:n.114-3756A>C
ENST00000464251.5:c.806-414A>C	ENSP00000428980.1:n.806-414A>C
ENST00000466323.5:c.*71-414A>C	ENSP00000418264.1:n.*71-414A>C
ENST00000490775.5:n.665-414A>C
NM_000202.6:c.880-414A>C	NP_000193.1:n.880-414A>C
NM_001166550.2:c.610-414A>C	NP_001160022.1:n.610-414A>C
NM_006123.4:c.880-414A>C	NP_006114.1:n.880-414A>C
NR_104128.1:n.1227-414A>C
NM_000202.7:c.880-414A>C	NP_000193.1:n.880-414A>C
NM_001166550.3:c.610-414A>C	NP_001160022.1:n.610-414A>C
NM_000202.8:c.880-414A>C MANE Select	NP_000193.1:n.880-414A>C
NM_001166550.4:c.610-414A>C	NP_001160022.1:n.610-414A>C
NM_006123.5:c.880-414A>C	NP_006114.1:n.880-414A>C
NR_104128.2:n.1179-414A>C