Canonical Allele Identifier: CA2694908963

Gene: IDS

Linked Data

• gnomAD v4: X-149483248-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483250del , CM000685.2:g.149483250del	GRCh38
NC_000023.10:g.148564781del , CM000685.1:g.148564781del	GRCh37
NC_000023.9:g.148372686del	NCBI36
NG_011900.3:g.27086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-31del MANE Select	ENSP00000339801.6:n.1181-31del
ENST00000651111.1:c.548-31del	ENSP00000498395.1:n.548-31del
ENST00000340855.10:c.1181-31del	ENSP00000339801.6:n.1181-31del
ENST00000422081.6:c.548-31del	ENSP00000477056.1:n.548-31del
ENST00000441880.1:n.288-31del
NM_000202.6:c.1181-31del	NP_000193.1:n.1181-31del
NM_001166550.2:c.911-31del	NP_001160022.1:n.911-31del
NM_000202.7:c.1181-31del	NP_000193.1:n.1181-31del
NM_001166550.3:c.911-31del	NP_001160022.1:n.911-31del
NM_000202.8:c.1181-31del MANE Select	NP_000193.1:n.1181-31del
NM_001166550.4:c.911-31del	NP_001160022.1:n.911-31del