Canonical Allele Identifier: CA414518045

Gene: IDS

Linked Data

• gnomAD v4: X-149482941-C-A
• MyVariant Identifiers: chrX:g.148564472C>A (hg19) ; chrX:g.149482941C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482941C>A , CM000685.2:g.149482941C>A	GRCh38
NC_000023.10:g.148564472C>A , CM000685.1:g.148564472C>A	GRCh37
NC_000023.9:g.148372377C>A	NCBI36
NG_011900.3:g.27394G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.1458G>T MANE Select	ENSP00000339801.6:p.Lys486Asn
ENST00000651111.1:c.825G>T	ENSP00000498395.1:p.Lys275Asn
ENST00000340855.10:c.1458G>T	ENSP00000339801.6:p.Lys486Asn
ENST00000422081.6:c.825G>T	ENSP00000477056.1:p.Lys275Asn
NM_000202.6:c.1458G>T	NP_000193.1:p.Lys486Asn
NM_001166550.2:c.1188G>T	NP_001160022.1:p.Lys396Asn
NM_000202.7:c.1458G>T	NP_000193.1:p.Lys486Asn
NM_001166550.3:c.1188G>T	NP_001160022.1:p.Lys396Asn
NM_000202.8:c.1458G>T MANE Select	NP_000193.1:p.Lys486Asn
NM_001166550.4:c.1188G>T	NP_001160022.1:p.Lys396Asn