Canonical Allele Identifier: CA2694898048

Gene: IDS

Linked Data

• gnomAD v4: X-149496645-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496649del , CM000685.2:g.149496649del	GRCh38
NC_000023.10:g.148578180del , CM000685.1:g.148578180del	GRCh37
NC_000023.9:g.148386085del	NCBI36
NG_011900.3:g.13689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-130del MANE Select	ENSP00000339801.6:n.709-130del
ENST00000651111.1:c.76-130del	ENSP00000498395.1:n.76-130del
ENST00000340855.10:c.709-130del	ENSP00000339801.6:n.709-130del
ENST00000370441.8:c.709-130del	ENSP00000359470.4:n.709-130del
ENST00000422081.6:c.76-130del	ENSP00000477056.1:n.76-130del
ENST00000441880.1:n.114-9548del
ENST00000464251.5:c.635-130del	ENSP00000428980.1:n.635-130del
ENST00000466019.1:n.161-130del
ENST00000466323.5:c.709-130del	ENSP00000418264.1:n.709-130del
ENST00000490775.5:n.494-130del
NM_000202.6:c.709-130del	NP_000193.1:n.709-130del
NM_001166550.2:c.439-130del	NP_001160022.1:n.439-130del
NM_006123.4:c.709-130del	NP_006114.1:n.709-130del
NR_104128.1:n.926-130del
NM_000202.7:c.709-130del	NP_000193.1:n.709-130del
NM_001166550.3:c.439-130del	NP_001160022.1:n.439-130del
NM_000202.8:c.709-130del MANE Select	NP_000193.1:n.709-130del
NM_001166550.4:c.439-130del	NP_001160022.1:n.439-130del
NM_006123.5:c.709-130del	NP_006114.1:n.709-130del
NR_104128.2:n.878-130del