Canonical Allele Identifier: CA2465003952

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482850T= , CM000685.2:g.149482850T=	GRCh38
NC_000023.10:g.148564381T= , CM000685.1:g.148564381T=	GRCh37
NC_000023.9:g.148372286T=	NCBI36
NG_011900.3:g.27485A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1549A= MANE Select	ENSP00000339801.6:p.Ile517=
ENST00000651111.1:c.916A=	ENSP00000498395.1:p.Ile306=
ENST00000340855.10:c.1549A=	ENSP00000339801.6:p.Ile517=
ENST00000422081.6:c.916A=	ENSP00000477056.1:p.Ile306=
NM_000202.6:c.1549A=	NP_000193.1:p.Ile517=
NM_001166550.2:c.1279A=	NP_001160022.1:p.Ile427=
NM_000202.7:c.1549A=	NP_000193.1:p.Ile517=
NM_001166550.3:c.1279A=	NP_001160022.1:p.Ile427=
NM_000202.8:c.1549A= MANE Select	NP_000193.1:p.Ile517=
NM_001166550.4:c.1279A=	NP_001160022.1:p.Ile427=