Canonical Allele Identifier: CA2695236510

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486993_149487012del , CM000685.2:g.149486993_149487012del	GRCh38
NC_000023.10:g.148568524_148568543del , CM000685.1:g.148568524_148568543del	GRCh37
NC_000023.9:g.148376429_148376448del	NCBI36
NG_011900.3:g.23326_23345del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1096_1115del MANE Select	ENSP00000339801.6:p.Arg366GlyfsTer13
ENST00000651111.1:c.463_482del	ENSP00000498395.1:p.Arg155GlyfsTer13
ENST00000340855.10:c.1096_1115del	ENSP00000339801.6:p.Arg366GlyfsTer13
ENST00000422081.6:c.463_482del	ENSP00000477056.1:p.Arg155GlyfsTer13
ENST00000441880.1:n.203_222del
NM_000202.6:c.1096_1115del	NP_000193.1:p.Arg366GlyfsTer13
NM_001166550.2:c.826_845del	NP_001160022.1:p.Arg276GlyfsTer13
NM_000202.7:c.1096_1115del	NP_000193.1:p.Arg366GlyfsTer13
NM_001166550.3:c.826_845del	NP_001160022.1:p.Arg276GlyfsTer13
NM_000202.8:c.1096_1115del MANE Select	NP_000193.1:p.Arg366GlyfsTer13
NM_001166550.4:c.826_845del	NP_001160022.1:p.Arg276GlyfsTer13