Canonical Allele Identifier: CA2465004061

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483135A= , CM000685.2:g.149483135A=	GRCh38
NC_000023.10:g.148564666A= , CM000685.1:g.148564666A=	GRCh37
NC_000023.9:g.148372571A=	NCBI36
NG_011900.3:g.27200T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1264T= MANE Select	ENSP00000339801.6:p.Cys422=
ENST00000651111.1:c.631T=	ENSP00000498395.1:p.Cys211=
ENST00000340855.10:c.1264T=	ENSP00000339801.6:p.Cys422=
ENST00000422081.6:c.631T=	ENSP00000477056.1:p.Cys211=
ENST00000441880.1:n.371T=
NM_000202.6:c.1264T=	NP_000193.1:p.Cys422=
NM_001166550.2:c.994T=	NP_001160022.1:p.Cys332=
NM_000202.7:c.1264T=	NP_000193.1:p.Cys422=
NM_001166550.3:c.994T=	NP_001160022.1:p.Cys332=
NM_000202.8:c.1264T= MANE Select	NP_000193.1:p.Cys422=
NM_001166550.4:c.994T=	NP_001160022.1:p.Cys332=