Canonical Allele Identifier: CA2695236652

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498221_149498225delinsTGTCA , CM000685.2:g.149498221_149498225delinsTGTCA	GRCh38
NC_000023.10:g.148579752_148579756delinsTGTCA , CM000685.1:g.148579752_148579756delinsTGTCA	GRCh37
NC_000023.9:g.148387657_148387661delinsTGTCA	NCBI36
NG_011900.3:g.12110_12114delinsTGACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.590_594delinsTGACA MANE Select	ENSP00000339801.6:p.Pro197_Asp198delinsLeuThr
ENST00000651111.1:c.-44_-40delinsTGACA	ENSP00000498395.1:n.-44_-40delinsTGACA
ENST00000340855.10:c.590_594delinsTGACA	ENSP00000339801.6:p.Pro197_Asp198delinsLeuThr
ENST00000370441.8:c.590_594delinsTGACA	ENSP00000359470.4:p.Pro197_Asp198delinsLeuThr
ENST00000422081.6:c.-44_-40delinsTGACA	ENSP00000477056.1:n.-44_-40delinsTGACA
ENST00000441880.1:n.114-11127_114-11123delinsTGACA
ENST00000464251.5:c.516_520delinsTGACA	ENSP00000428980.1:n.516_520delinsTGACA
ENST00000466019.1:n.42_46delinsTGACA
ENST00000466323.5:c.590_594delinsTGACA	ENSP00000418264.1:p.Pro197_Asp198delinsLeuThr
ENST00000490775.5:n.375_379delinsTGACA
ENST00000523759.5:n.704_708delinsTGACA
NM_000202.6:c.590_594delinsTGACA	NP_000193.1:p.Pro197_Asp198delinsLeuThr
NM_001166550.2:c.320_324delinsTGACA	NP_001160022.1:p.Pro107_Asp108delinsLeuThr
NM_006123.4:c.590_594delinsTGACA	NP_006114.1:p.Pro197_Asp198delinsLeuThr
NR_104128.1:n.807_811delinsTGACA
NM_000202.7:c.590_594delinsTGACA	NP_000193.1:p.Pro197_Asp198delinsLeuThr
NM_001166550.3:c.320_324delinsTGACA	NP_001160022.1:p.Pro107_Asp108delinsLeuThr
NM_000202.8:c.590_594delinsTGACA MANE Select	NP_000193.1:p.Pro197_Asp198delinsLeuThr
NM_001166550.4:c.320_324delinsTGACA	NP_001160022.1:p.Pro107_Asp108delinsLeuThr
NM_006123.5:c.590_594delinsTGACA	NP_006114.1:p.Pro197_Asp198delinsLeuThr
NR_104128.2:n.759_763delinsTGACA