Canonical Allele Identifier: CA2465008736

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496540A= , CM000685.2:g.149496540A=	GRCh38
NC_000023.10:g.148578071A= , CM000685.1:g.148578071A=	GRCh37
NC_000023.9:g.148385976A=	NCBI36
NG_011900.3:g.13795T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-24T= MANE Select	ENSP00000339801.6:n.709-24T=
ENST00000651111.1:c.76-24T=	ENSP00000498395.1:n.76-24T=
ENST00000340855.10:c.709-24T=	ENSP00000339801.6:n.709-24T=
ENST00000370441.8:c.709-24T=	ENSP00000359470.4:n.709-24T=
ENST00000422081.6:c.76-24T=	ENSP00000477056.1:n.76-24T=
ENST00000441880.1:n.114-9442T=
ENST00000464251.5:c.635-24T=	ENSP00000428980.1:n.635-24T=
ENST00000466019.1:n.161-24T=
ENST00000466323.5:c.709-24T=	ENSP00000418264.1:n.709-24T=
ENST00000490775.5:n.494-24T=
NM_000202.6:c.709-24T=	NP_000193.1:n.709-24T=
NM_001166550.2:c.439-24T=	NP_001160022.1:n.439-24T=
NM_006123.4:c.709-24T=	NP_006114.1:n.709-24T=
NR_104128.1:n.926-24T=
NM_000202.7:c.709-24T=	NP_000193.1:n.709-24T=
NM_001166550.3:c.439-24T=	NP_001160022.1:n.439-24T=
NM_000202.8:c.709-24T= MANE Select	NP_000193.1:n.709-24T=
NM_001166550.4:c.439-24T=	NP_001160022.1:n.439-24T=
NM_006123.5:c.709-24T=	NP_006114.1:n.709-24T=
NR_104128.2:n.878-24T=