Canonical Allele Identifier: CA2739144666

Gene: IDS

Linked Data

• dbSNP Id: rs2124042364

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496583_149496584del , CM000685.2:g.149496583_149496584del	GRCh38
NC_000023.10:g.148578114_148578115del , CM000685.1:g.148578114_148578115del	GRCh37
NC_000023.9:g.148386019_148386020del	NCBI36
NG_011900.3:g.13751_13752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-68_709-67del MANE Select	ENSP00000339801.6:n.709-68_709-67del
ENST00000651111.1:c.76-68_76-67del	ENSP00000498395.1:n.76-68_76-67del
ENST00000340855.10:c.709-68_709-67del	ENSP00000339801.6:n.709-68_709-67del
ENST00000370441.8:c.709-68_709-67del	ENSP00000359470.4:n.709-68_709-67del
ENST00000422081.6:c.76-68_76-67del	ENSP00000477056.1:n.76-68_76-67del
ENST00000441880.1:n.114-9486_114-9485del
ENST00000464251.5:c.635-68_635-67del	ENSP00000428980.1:n.635-68_635-67del
ENST00000466019.1:n.161-68_161-67del
ENST00000466323.5:c.709-68_709-67del	ENSP00000418264.1:n.709-68_709-67del
ENST00000490775.5:n.494-68_494-67del
NM_000202.6:c.709-68_709-67del	NP_000193.1:n.709-68_709-67del
NM_001166550.2:c.439-68_439-67del	NP_001160022.1:n.439-68_439-67del
NM_006123.4:c.709-68_709-67del	NP_006114.1:n.709-68_709-67del
NR_104128.1:n.926-68_926-67del
NM_000202.7:c.709-68_709-67del	NP_000193.1:n.709-68_709-67del
NM_001166550.3:c.439-68_439-67del	NP_001160022.1:n.439-68_439-67del
NM_000202.8:c.709-68_709-67del MANE Select	NP_000193.1:n.709-68_709-67del
NM_001166550.4:c.439-68_439-67del	NP_001160022.1:n.439-68_439-67del
NM_006123.5:c.709-68_709-67del	NP_006114.1:n.709-68_709-67del
NR_104128.2:n.878-68_878-67del