Canonical Allele Identifier: CA519060956

Gene: IDS

Linked Data

• dbSNP Id: rs2089496498
• gnomAD v4: X-149503412-G-A
• MyVariant Identifiers: chrX:g.148584942G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503412G>A , CM000685.2:g.149503412G>A	GRCh38
NC_000023.10:g.148584942G>A , CM000685.1:g.148584942G>A	GRCh37
NC_000023.9:g.148392847G>A	NCBI36
NG_011900.3:g.6923C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.318C>T MANE Select	ENSP00000339801.6:p.Asn106=
ENST00000651111.1:c.-215-2375C>T	ENSP00000498395.1:n.-215-2375C>T
ENST00000340855.10:c.318C>T	ENSP00000339801.6:p.Asn106=
ENST00000370441.8:c.318C>T	ENSP00000359470.4:p.Asn106=
ENST00000422081.6:c.-215-2375C>T	ENSP00000477056.1:n.-215-2375C>T
ENST00000427113.2:n.770-1189C>T
ENST00000428056.6:c.318C>T	ENSP00000390241.2:p.Asn106=
ENST00000441880.1:n.114-16314C>T
ENST00000464251.5:c.141C>T	ENSP00000428980.1:p.Asn47=
ENST00000466323.5:c.318C>T	ENSP00000418264.1:p.Asn106=
ENST00000523759.5:n.533-2375C>T
NM_000202.6:c.318C>T	NP_000193.1:p.Asn106=
NM_001166550.2:c.48C>T	NP_001160022.1:p.Asn16=
NM_006123.4:c.318C>T	NP_006114.1:p.Asn106=
NR_104128.1:n.535C>T
NM_000202.7:c.318C>T	NP_000193.1:p.Asn106=
NM_001166550.3:c.48C>T	NP_001160022.1:p.Asn16=
NM_000202.8:c.318C>T MANE Select	NP_000193.1:p.Asn106=
NM_001166550.4:c.48C>T	NP_001160022.1:p.Asn16=
NM_006123.5:c.318C>T	NP_006114.1:p.Asn106=
NR_104128.2:n.487C>T