Canonical Allele Identifier: CA2694909064

Gene: IDS

Linked Data

• gnomAD v4: X-149486877-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486877T>G , CM000685.2:g.149486877T>G	GRCh38
NC_000023.10:g.148568408T>G , CM000685.1:g.148568408T>G	GRCh37
NC_000023.9:g.148376313T>G	NCBI36
NG_011900.3:g.23458A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1180+48A>C MANE Select	ENSP00000339801.6:n.1180+48A>C
ENST00000651111.1:c.547+48A>C	ENSP00000498395.1:n.547+48A>C
ENST00000340855.10:c.1180+48A>C	ENSP00000339801.6:n.1180+48A>C
ENST00000422081.6:c.547+48A>C	ENSP00000477056.1:n.547+48A>C
ENST00000441880.1:n.287+48A>C
NM_000202.6:c.1180+48A>C	NP_000193.1:n.1180+48A>C
NM_001166550.2:c.910+48A>C	NP_001160022.1:n.910+48A>C
NM_000202.7:c.1180+48A>C	NP_000193.1:n.1180+48A>C
NM_001166550.3:c.910+48A>C	NP_001160022.1:n.910+48A>C
NM_000202.8:c.1180+48A>C MANE Select	NP_000193.1:n.1180+48A>C
NM_001166550.4:c.910+48A>C	NP_001160022.1:n.910+48A>C