Canonical Allele Identifier: CA519057636

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148568622A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487091A>C , CM000685.2:g.149487091A>C	GRCh38
NC_000023.10:g.148568622A>C , CM000685.1:g.148568622A>C	GRCh37
NC_000023.9:g.148376527A>C	NCBI36
NG_011900.3:g.23244T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1014T>G MANE Select	ENSP00000339801.6:p.Ala338=
ENST00000651111.1:c.381T>G	ENSP00000498395.1:p.Ala127=
ENST00000340855.10:c.1014T>G	ENSP00000339801.6:p.Ala338=
ENST00000422081.6:c.381T>G	ENSP00000477056.1:p.Ala127=
ENST00000441880.1:n.121T>G
NM_000202.6:c.1014T>G	NP_000193.1:p.Ala338=
NM_001166550.2:c.744T>G	NP_001160022.1:p.Ala248=
NM_000202.7:c.1014T>G	NP_000193.1:p.Ala338=
NM_001166550.3:c.744T>G	NP_001160022.1:p.Ala248=
NM_000202.8:c.1014T>G MANE Select	NP_000193.1:p.Ala338=
NM_001166550.4:c.744T>G	NP_001160022.1:p.Ala248=