Canonical Allele Identifier: CA2465003964

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482895A= , CM000685.2:g.149482895A=	GRCh38
NC_000023.10:g.148564426A= , CM000685.1:g.148564426A=	GRCh37
NC_000023.9:g.148372331A=	NCBI36
NG_011900.3:g.27440T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1504T= MANE Select	ENSP00000339801.6:p.Trp502=
ENST00000651111.1:c.871T=	ENSP00000498395.1:p.Trp291=
ENST00000340855.10:c.1504T=	ENSP00000339801.6:p.Trp502=
ENST00000422081.6:c.871T=	ENSP00000477056.1:p.Trp291=
NM_000202.6:c.1504T=	NP_000193.1:p.Trp502=
NM_001166550.2:c.1234T=	NP_001160022.1:p.Trp412=
NM_000202.7:c.1504T=	NP_000193.1:p.Trp502=
NM_001166550.3:c.1234T=	NP_001160022.1:p.Trp412=
NM_000202.8:c.1504T= MANE Select	NP_000193.1:p.Trp502=
NM_001166550.4:c.1234T=	NP_001160022.1:p.Trp412=