Canonical Allele Identifier: CA519173926

Gene: IDS

Linked Data

• ClinVar Variation Id: 2881387
• ClinVar RCV Id: RCV003623669
• MyVariant Identifiers: chrX:g.148564559G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483028G>C , CM000685.2:g.149483028G>C	GRCh38
NC_000023.10:g.148564559G>C , CM000685.1:g.148564559G>C	GRCh37
NC_000023.9:g.148372464G>C	NCBI36
NG_011900.3:g.27307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1371C>G MANE Select	ENSP00000339801.6:p.Pro457=
ENST00000651111.1:c.738C>G	ENSP00000498395.1:p.Pro246=
ENST00000340855.10:c.1371C>G	ENSP00000339801.6:p.Pro457=
ENST00000422081.6:c.738C>G	ENSP00000477056.1:p.Pro246=
NM_000202.6:c.1371C>G	NP_000193.1:p.Pro457=
NM_001166550.2:c.1101C>G	NP_001160022.1:p.Pro367=
NM_000202.7:c.1371C>G	NP_000193.1:p.Pro457=
NM_001166550.3:c.1101C>G	NP_001160022.1:p.Pro367=
NM_000202.8:c.1371C>G MANE Select	NP_000193.1:p.Pro457=
NM_001166550.4:c.1101C>G	NP_001160022.1:p.Pro367=