Canonical Allele Identifier: CA2465006803

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490436T= , CM000685.2:g.149490436T=	GRCh38
NC_000023.10:g.148571967T= , CM000685.1:g.148571967T=	GRCh37
NC_000023.9:g.148379872T=	NCBI36
NG_011900.3:g.19899A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000202.8:c.884A= MANE Select	NP_000193.1:p.Lys295=
ENST00000340855.11:c.884A= MANE Select	ENSP00000339801.6:p.Lys295=
NM_000202.6:c.884A=	NP_000193.1:p.Lys295=
NM_000202.7:c.884A=	NP_000193.1:p.Lys295=
NM_001166550.2:c.614A=	NP_001160022.1:p.Lys205=
NM_001166550.3:c.614A=	NP_001160022.1:p.Lys205=
NM_001166550.4:c.614A=	NP_001160022.1:p.Lys205=
NM_006123.4:c.884A=	NP_006114.1:p.Lys295=
NM_006123.5:c.884A=	NP_006114.1:p.Lys295=
NR_104128.1:n.1231A=
NR_104128.2:n.1183A=
ENST00000340855.10:c.884A=	ENSP00000339801.6:p.Lys295=
ENST00000370441.8:c.884A=	ENSP00000359470.4:p.Lys295=
ENST00000422081.6:c.251A=	ENSP00000477056.1:p.Lys84=
ENST00000441880.1:n.114-3338A=
ENST00000464251.5:c.810A=	ENSP00000428980.1:n.810A=
ENST00000466323.5:c.*75A=	ENSP00000418264.1:n.*75A=
ENST00000490775.5:n.669A=
ENST00000651111.1:c.251A=	ENSP00000498395.1:p.Lys84=