Canonical Allele Identifier: CA2465005671

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487248C= , CM000685.2:g.149487248C=	GRCh38
NC_000023.10:g.148568779C= , CM000685.1:g.148568779C=	GRCh37
NC_000023.9:g.148376684C=	NCBI36
NG_011900.3:g.23087G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-150G= MANE Select	ENSP00000339801.6:n.1007-150G=
ENST00000651111.1:c.374-150G=	ENSP00000498395.1:n.374-150G=
ENST00000340855.10:c.1007-150G=	ENSP00000339801.6:n.1007-150G=
ENST00000370441.8:c.*40G=	ENSP00000359470.4:n.*40G=
ENST00000422081.6:c.374-150G=	ENSP00000477056.1:n.374-150G=
ENST00000441880.1:n.114-150G=
ENST00000466323.5:c.*263G=	ENSP00000418264.1:n.*263G=
ENST00000490775.5:n.857G=
NM_000202.6:c.1007-150G=	NP_000193.1:n.1007-150G=
NM_001166550.2:c.737-150G=	NP_001160022.1:n.737-150G=
NM_006123.4:c.*40G=	NP_006114.1:n.*40G=
NR_104128.1:n.1419G=
NM_000202.7:c.1007-150G=	NP_000193.1:n.1007-150G=
NM_001166550.3:c.737-150G=	NP_001160022.1:n.737-150G=
NM_000202.8:c.1007-150G= MANE Select	NP_000193.1:n.1007-150G=
NM_001166550.4:c.737-150G=	NP_001160022.1:n.737-150G=
NM_006123.5:c.*40G=	NP_006114.1:n.*40G=
NR_104128.2:n.1371G=