Canonical Allele Identifier: CA2465003947

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482831T= , CM000685.2:g.149482831T=	GRCh38
NC_000023.10:g.148564362T= , CM000685.1:g.148564362T=	GRCh37
NC_000023.9:g.148372267T=	NCBI36
NG_011900.3:g.27504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1568A= MANE Select	ENSP00000339801.6:p.Tyr523=
ENST00000651111.1:c.935A=	ENSP00000498395.1:p.Tyr312=
ENST00000340855.10:c.1568A=	ENSP00000339801.6:p.Tyr523=
ENST00000422081.6:c.935A=	ENSP00000477056.1:p.Tyr312=
NM_000202.6:c.1568A=	NP_000193.1:p.Tyr523=
NM_001166550.2:c.1298A=	NP_001160022.1:p.Tyr433=
NM_000202.7:c.1568A=	NP_000193.1:p.Tyr523=
NM_001166550.3:c.1298A=	NP_001160022.1:p.Tyr433=
NM_000202.8:c.1568A= MANE Select	NP_000193.1:p.Tyr523=
NM_001166550.4:c.1298A=	NP_001160022.1:p.Tyr433=