Canonical Allele Identifier: CA872890265

Gene: IDS

Linked Data

• dbSNP Id: rs1163836632
• gnomAD v3: X-149483418-A-G
• gnomAD v4: X-149483418-A-G
• MyVariant Identifiers: chrX:g.149483418A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483418A>G , CM000685.2:g.149483418A>G	GRCh38
NC_000023.10:g.148564949A>G , CM000685.1:g.148564949A>G	GRCh37
NC_000023.9:g.148372854A>G	NCBI36
NG_011900.3:g.26917T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-200T>C MANE Select	ENSP00000339801.6:n.1181-200T>C
ENST00000651111.1:c.548-200T>C	ENSP00000498395.1:n.548-200T>C
ENST00000340855.10:c.1181-200T>C	ENSP00000339801.6:n.1181-200T>C
ENST00000422081.6:c.548-200T>C	ENSP00000477056.1:n.548-200T>C
ENST00000441880.1:n.288-200T>C
NM_000202.6:c.1181-200T>C	NP_000193.1:n.1181-200T>C
NM_001166550.2:c.911-200T>C	NP_001160022.1:n.911-200T>C
NM_000202.7:c.1181-200T>C	NP_000193.1:n.1181-200T>C
NM_001166550.3:c.911-200T>C	NP_001160022.1:n.911-200T>C
NM_000202.8:c.1181-200T>C MANE Select	NP_000193.1:n.1181-200T>C
NM_001166550.4:c.911-200T>C	NP_001160022.1:n.911-200T>C