Canonical Allele Identifier: CA2465009212

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498149G= , CM000685.2:g.149498149G=	GRCh38
NC_000023.10:g.148579680G= , CM000685.1:g.148579680G=	GRCh37
NC_000023.9:g.148387585G=	NCBI36
NG_011900.3:g.12186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.666C= MANE Select	ENSP00000339801.6:p.Ala222=
ENST00000651111.1:c.33C=	ENSP00000498395.1:p.Ala11=
ENST00000340855.10:c.666C=	ENSP00000339801.6:p.Ala222=
ENST00000370441.8:c.666C=	ENSP00000359470.4:p.Ala222=
ENST00000422081.6:c.33C=	ENSP00000477056.1:p.Ala11=
ENST00000441880.1:n.114-11051C=
ENST00000464251.5:c.592C=	ENSP00000428980.1:n.592C=
ENST00000466019.1:n.118C=
ENST00000466323.5:c.666C=	ENSP00000418264.1:p.Ala222=
ENST00000490775.5:n.451C=
NM_000202.6:c.666C=	NP_000193.1:p.Ala222=
NM_001166550.2:c.396C=	NP_001160022.1:p.Ala132=
NM_006123.4:c.666C=	NP_006114.1:p.Ala222=
NR_104128.1:n.883C=
NM_000202.7:c.666C=	NP_000193.1:p.Ala222=
NM_001166550.3:c.396C=	NP_001160022.1:p.Ala132=
NM_000202.8:c.666C= MANE Select	NP_000193.1:p.Ala222=
NM_001166550.4:c.396C=	NP_001160022.1:p.Ala132=
NM_006123.5:c.666C=	NP_006114.1:p.Ala222=
NR_104128.2:n.835C=