Canonical Allele Identifier: CA2465009218

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498177T= , CM000685.2:g.149498177T=	GRCh38
NC_000023.10:g.148579708T= , CM000685.1:g.148579708T=	GRCh37
NC_000023.9:g.148387613T=	NCBI36
NG_011900.3:g.12158A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.638A= MANE Select	ENSP00000339801.6:p.Lys213=
ENST00000651111.1:c.5A=	ENSP00000498395.1:p.Lys2=
ENST00000340855.10:c.638A=	ENSP00000339801.6:p.Lys213=
ENST00000370441.8:c.638A=	ENSP00000359470.4:p.Lys213=
ENST00000422081.6:c.5A=	ENSP00000477056.1:p.Lys2=
ENST00000441880.1:n.114-11079A=
ENST00000464251.5:c.564A=	ENSP00000428980.1:n.564A=
ENST00000466019.1:n.90A=
ENST00000466323.5:c.638A=	ENSP00000418264.1:p.Lys213=
ENST00000490775.5:n.423A=
NM_000202.6:c.638A=	NP_000193.1:p.Lys213=
NM_001166550.2:c.368A=	NP_001160022.1:p.Lys123=
NM_006123.4:c.638A=	NP_006114.1:p.Lys213=
NR_104128.1:n.855A=
NM_000202.7:c.638A=	NP_000193.1:p.Lys213=
NM_001166550.3:c.368A=	NP_001160022.1:p.Lys123=
NM_000202.8:c.638A= MANE Select	NP_000193.1:p.Lys213=
NM_001166550.4:c.368A=	NP_001160022.1:p.Lys123=
NM_006123.5:c.638A=	NP_006114.1:p.Lys213=
NR_104128.2:n.807A=