Canonical Allele Identifier: CA2694909003

Gene: IDS

Linked Data

• gnomAD v4: X-149483325-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483325T>C , CM000685.2:g.149483325T>C	GRCh38
NC_000023.10:g.148564856T>C , CM000685.1:g.148564856T>C	GRCh37
NC_000023.9:g.148372761T>C	NCBI36
NG_011900.3:g.27010A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-107A>G MANE Select	ENSP00000339801.6:n.1181-107A>G
ENST00000651111.1:c.548-107A>G	ENSP00000498395.1:n.548-107A>G
ENST00000340855.10:c.1181-107A>G	ENSP00000339801.6:n.1181-107A>G
ENST00000422081.6:c.548-107A>G	ENSP00000477056.1:n.548-107A>G
ENST00000441880.1:n.288-107A>G
NM_000202.6:c.1181-107A>G	NP_000193.1:n.1181-107A>G
NM_001166550.2:c.911-107A>G	NP_001160022.1:n.911-107A>G
NM_000202.7:c.1181-107A>G	NP_000193.1:n.1181-107A>G
NM_001166550.3:c.911-107A>G	NP_001160022.1:n.911-107A>G
NM_000202.8:c.1181-107A>G MANE Select	NP_000193.1:n.1181-107A>G
NM_001166550.4:c.911-107A>G	NP_001160022.1:n.911-107A>G