Canonical Allele Identifier: CA2465009208

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498137A= , CM000685.2:g.149498137A=	GRCh38
NC_000023.10:g.148579668A= , CM000685.1:g.148579668A=	GRCh37
NC_000023.9:g.148387573A=	NCBI36
NG_011900.3:g.12198T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.678T= MANE Select	ENSP00000339801.6:p.His226=
ENST00000651111.1:c.45T=	ENSP00000498395.1:p.His15=
ENST00000340855.10:c.678T=	ENSP00000339801.6:p.His226=
ENST00000370441.8:c.678T=	ENSP00000359470.4:p.His226=
ENST00000422081.6:c.45T=	ENSP00000477056.1:p.His15=
ENST00000441880.1:n.114-11039T=
ENST00000464251.5:c.604T=	ENSP00000428980.1:n.604T=
ENST00000466019.1:n.130T=
ENST00000466323.5:c.678T=	ENSP00000418264.1:p.His226=
ENST00000490775.5:n.463T=
NM_000202.6:c.678T=	NP_000193.1:p.His226=
NM_001166550.2:c.408T=	NP_001160022.1:p.His136=
NM_006123.4:c.678T=	NP_006114.1:p.His226=
NR_104128.1:n.895T=
NM_000202.7:c.678T=	NP_000193.1:p.His226=
NM_001166550.3:c.408T=	NP_001160022.1:p.His136=
NM_000202.8:c.678T= MANE Select	NP_000193.1:p.His226=
NM_001166550.4:c.408T=	NP_001160022.1:p.His136=
NM_006123.5:c.678T=	NP_006114.1:p.His226=
NR_104128.2:n.847T=