Canonical Allele Identifier: CA2465005611

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487134A= , CM000685.2:g.149487134A=	GRCh38
NC_000023.10:g.148568665A= , CM000685.1:g.148568665A=	GRCh37
NC_000023.9:g.148376570A=	NCBI36
NG_011900.3:g.23201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-36T= MANE Select	ENSP00000339801.6:n.1007-36T=
ENST00000651111.1:c.374-36T=	ENSP00000498395.1:n.374-36T=
ENST00000340855.10:c.1007-36T=	ENSP00000339801.6:n.1007-36T=
ENST00000370441.8:c.*154T=	ENSP00000359470.4:n.*154T=
ENST00000422081.6:c.374-36T=	ENSP00000477056.1:n.374-36T=
ENST00000441880.1:n.114-36T=
ENST00000466323.5:c.*377T=	ENSP00000418264.1:n.*377T=
NM_000202.6:c.1007-36T=	NP_000193.1:n.1007-36T=
NM_001166550.2:c.737-36T=	NP_001160022.1:n.737-36T=
NM_006123.4:c.*154T=	NP_006114.1:n.*154T=
NR_104128.1:n.1533T=
NM_000202.7:c.1007-36T=	NP_000193.1:n.1007-36T=
NM_001166550.3:c.737-36T=	NP_001160022.1:n.737-36T=
NM_000202.8:c.1007-36T= MANE Select	NP_000193.1:n.1007-36T=
NM_001166550.4:c.737-36T=	NP_001160022.1:n.737-36T=
NM_006123.5:c.*154T=	NP_006114.1:n.*154T=
NR_104128.2:n.1485T=