Canonical Allele Identifier: CA2465004171

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483443T= , CM000685.2:g.149483443T=	GRCh38
NC_000023.10:g.148564974T= , CM000685.1:g.148564974T=	GRCh37
NC_000023.9:g.148372879T=	NCBI36
NG_011900.3:g.26892A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-225A= MANE Select	ENSP00000339801.6:n.1181-225A=
ENST00000651111.1:c.548-225A=	ENSP00000498395.1:n.548-225A=
ENST00000340855.10:c.1181-225A=	ENSP00000339801.6:n.1181-225A=
ENST00000422081.6:c.548-225A=	ENSP00000477056.1:n.548-225A=
ENST00000441880.1:n.288-225A=
NM_000202.6:c.1181-225A=	NP_000193.1:n.1181-225A=
NM_001166550.2:c.911-225A=	NP_001160022.1:n.911-225A=
NM_000202.7:c.1181-225A=	NP_000193.1:n.1181-225A=
NM_001166550.3:c.911-225A=	NP_001160022.1:n.911-225A=
NM_000202.8:c.1181-225A= MANE Select	NP_000193.1:n.1181-225A=
NM_001166550.4:c.911-225A=	NP_001160022.1:n.911-225A=