Canonical Allele Identifier: CA2465005571

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486999G= , CM000685.2:g.149486999G=	GRCh38
NC_000023.10:g.148568530G= , CM000685.1:g.148568530G=	GRCh37
NC_000023.9:g.148376435G=	NCBI36
NG_011900.3:g.23336C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1106C= MANE Select	ENSP00000339801.6:p.Ser369=
ENST00000651111.1:c.473C=	ENSP00000498395.1:p.Ser158=
ENST00000340855.10:c.1106C=	ENSP00000339801.6:p.Ser369=
ENST00000422081.6:c.473C=	ENSP00000477056.1:p.Ser158=
ENST00000441880.1:n.213C=
NM_000202.6:c.1106C=	NP_000193.1:p.Ser369=
NM_001166550.2:c.836C=	NP_001160022.1:p.Ser279=
NM_000202.7:c.1106C=	NP_000193.1:p.Ser369=
NM_001166550.3:c.836C=	NP_001160022.1:p.Ser279=
NM_000202.8:c.1106C= MANE Select	NP_000193.1:p.Ser369=
NM_001166550.4:c.836C=	NP_001160022.1:p.Ser279=