Canonical Allele Identifier: CA2695236518

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483096_149483104del , CM000685.2:g.149483096_149483104del	GRCh38
NC_000023.10:g.148564627_148564635del , CM000685.1:g.148564627_148564635del	GRCh37
NC_000023.9:g.148372532_148372540del	NCBI36
NG_011900.3:g.27234_27242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1298_1306del MANE Select	ENSP00000339801.6:p.Arg433_Gly435del
ENST00000651111.1:c.665_673del	ENSP00000498395.1:p.Arg222_Gly224del
ENST00000340855.10:c.1298_1306del	ENSP00000339801.6:p.Arg433_Gly435del
ENST00000422081.6:c.665_673del	ENSP00000477056.1:p.Arg222_Gly224del
ENST00000441880.1:n.405_413del
NM_000202.6:c.1298_1306del	NP_000193.1:p.Arg433_Gly435del
NM_001166550.2:c.1028_1036del	NP_001160022.1:p.Arg343_Gly345del
NM_000202.7:c.1298_1306del	NP_000193.1:p.Arg433_Gly435del
NM_001166550.3:c.1028_1036del	NP_001160022.1:p.Arg343_Gly345del
NM_000202.8:c.1298_1306del MANE Select	NP_000193.1:p.Arg433_Gly435del
NM_001166550.4:c.1028_1036del	NP_001160022.1:p.Arg343_Gly345del