Canonical Allele Identifier: CA2579719263

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498324del , CM000685.2:g.149498324del	GRCh38
NC_000023.10:g.148579855del , CM000685.1:g.148579855del	GRCh37
NC_000023.9:g.148387760del	NCBI36
NG_011900.3:g.12012del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.508-16del MANE Select	ENSP00000339801.6:n.508-16del
ENST00000651111.1:c.-126-16del	ENSP00000498395.1:n.-126-16del
ENST00000340855.10:c.508-16del	ENSP00000339801.6:n.508-16del
ENST00000370441.8:c.508-16del	ENSP00000359470.4:n.508-16del
ENST00000422081.6:c.-126-16del	ENSP00000477056.1:n.-126-16del
ENST00000441880.1:n.114-11225del
ENST00000464251.5:c.434-16del	ENSP00000428980.1:n.434-16del
ENST00000466323.5:c.508-16del	ENSP00000418264.1:n.508-16del
ENST00000490775.5:n.293-16del
ENST00000523759.5:n.622-16del
NM_000202.6:c.508-16del	NP_000193.1:n.508-16del
NM_001166550.2:c.238-16del	NP_001160022.1:n.238-16del
NM_006123.4:c.508-16del	NP_006114.1:n.508-16del
NR_104128.1:n.725-16del
NM_000202.7:c.508-16del	NP_000193.1:n.508-16del
NM_001166550.3:c.238-16del	NP_001160022.1:n.238-16del
NM_000202.8:c.508-16del MANE Select	NP_000193.1:n.508-16del
NM_001166550.4:c.238-16del	NP_001160022.1:n.238-16del
NM_006123.5:c.508-16del	NP_006114.1:n.508-16del
NR_104128.2:n.677-16del