Canonical Allele Identifier: CA2694898144

Gene: IDS

Linked Data

• gnomAD v4: X-149498320-AATAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498325_149498329del , CM000685.2:g.149498325_149498329del	GRCh38
NC_000023.10:g.148579856_148579860del , CM000685.1:g.148579856_148579860del	GRCh37
NC_000023.9:g.148387761_148387765del	NCBI36
NG_011900.3:g.12010_12014del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.508-18_508-14del MANE Select	ENSP00000339801.6:n.508-18_508-14del
ENST00000651111.1:c.-126-18_-126-14del	ENSP00000498395.1:n.-126-18_-126-14del
ENST00000340855.10:c.508-18_508-14del	ENSP00000339801.6:n.508-18_508-14del
ENST00000370441.8:c.508-18_508-14del	ENSP00000359470.4:n.508-18_508-14del
ENST00000422081.6:c.-126-18_-126-14del	ENSP00000477056.1:n.-126-18_-126-14del
ENST00000441880.1:n.114-11227_114-11223del
ENST00000464251.5:c.434-18_434-14del	ENSP00000428980.1:n.434-18_434-14del
ENST00000466323.5:c.508-18_508-14del	ENSP00000418264.1:n.508-18_508-14del
ENST00000490775.5:n.293-18_293-14del
ENST00000523759.5:n.622-18_622-14del
NM_000202.6:c.508-18_508-14del	NP_000193.1:n.508-18_508-14del
NM_001166550.2:c.238-18_238-14del	NP_001160022.1:n.238-18_238-14del
NM_006123.4:c.508-18_508-14del	NP_006114.1:n.508-18_508-14del
NR_104128.1:n.725-18_725-14del
NM_000202.7:c.508-18_508-14del	NP_000193.1:n.508-18_508-14del
NM_001166550.3:c.238-18_238-14del	NP_001160022.1:n.238-18_238-14del
NM_000202.8:c.508-18_508-14del MANE Select	NP_000193.1:n.508-18_508-14del
NM_001166550.4:c.238-18_238-14del	NP_001160022.1:n.238-18_238-14del
NM_006123.5:c.508-18_508-14del	NP_006114.1:n.508-18_508-14del
NR_104128.2:n.677-18_677-14del