Canonical Allele Identifier: CA519057417
Gene: IDS HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.148564370C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482839C>A , CM000685.2:g.149482839C>A GRCh38
NC_000023.10:g.148564370C>A , CM000685.1:g.148564370C>A GRCh37
NC_000023.9:g.148372275C>A NCBI36
NG_011900.3:g.27496G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1560G>T MANE Select ENSP00000339801.6:p.Gly520=
ENST00000651111.1:c.927G>T ENSP00000498395.1:p.Gly309=
ENST00000340855.10:c.1560G>T ENSP00000339801.6:p.Gly520=
ENST00000422081.6:c.927G>T ENSP00000477056.1:p.Gly309=
NM_000202.6:c.1560G>T NP_000193.1:p.Gly520=
NM_001166550.2:c.1290G>T NP_001160022.1:p.Gly430=
NM_000202.7:c.1560G>T NP_000193.1:p.Gly520=
NM_001166550.3:c.1290G>T NP_001160022.1:p.Gly430=
NM_000202.8:c.1560G>T MANE Select NP_000193.1:p.Gly520=
NM_001166550.4:c.1290G>T NP_001160022.1:p.Gly430=