Canonical Allele Identifier: CA2465003984

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482941C= , CM000685.2:g.149482941C=	GRCh38
NC_000023.10:g.148564472C= , CM000685.1:g.148564472C=	GRCh37
NC_000023.9:g.148372377C=	NCBI36
NG_011900.3:g.27394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1458G= MANE Select	ENSP00000339801.6:p.Lys486=
ENST00000651111.1:c.825G=	ENSP00000498395.1:p.Lys275=
ENST00000340855.10:c.1458G=	ENSP00000339801.6:p.Lys486=
ENST00000422081.6:c.825G=	ENSP00000477056.1:p.Lys275=
NM_000202.6:c.1458G=	NP_000193.1:p.Lys486=
NM_001166550.2:c.1188G=	NP_001160022.1:p.Lys396=
NM_000202.7:c.1458G=	NP_000193.1:p.Lys486=
NM_001166550.3:c.1188G=	NP_001160022.1:p.Lys396=
NM_000202.8:c.1458G= MANE Select	NP_000193.1:p.Lys486=
NM_001166550.4:c.1188G=	NP_001160022.1:p.Lys396=