Canonical Allele Identifier: CA2465009204

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498129T= , CM000685.2:g.149498129T=	GRCh38
NC_000023.10:g.148579660T= , CM000685.1:g.148579660T=	GRCh37
NC_000023.9:g.148387565T=	NCBI36
NG_011900.3:g.12206A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.686A= MANE Select	ENSP00000339801.6:p.His229=
ENST00000651111.1:c.53A=	ENSP00000498395.1:p.His18=
ENST00000340855.10:c.686A=	ENSP00000339801.6:p.His229=
ENST00000370441.8:c.686A=	ENSP00000359470.4:p.His229=
ENST00000422081.6:c.53A=	ENSP00000477056.1:p.His18=
ENST00000441880.1:n.114-11031A=
ENST00000464251.5:c.612A=	ENSP00000428980.1:n.612A=
ENST00000466019.1:n.138A=
ENST00000466323.5:c.686A=	ENSP00000418264.1:p.His229=
ENST00000490775.5:n.471A=
NM_000202.6:c.686A=	NP_000193.1:p.His229=
NM_001166550.2:c.416A=	NP_001160022.1:p.His139=
NM_006123.4:c.686A=	NP_006114.1:p.His229=
NR_104128.1:n.903A=
NM_000202.7:c.686A=	NP_000193.1:p.His229=
NM_001166550.3:c.416A=	NP_001160022.1:p.His139=
NM_000202.8:c.686A= MANE Select	NP_000193.1:p.His229=
NM_001166550.4:c.416A=	NP_001160022.1:p.His139=
NM_006123.5:c.686A=	NP_006114.1:p.His229=
NR_104128.2:n.855A=