Canonical Allele Identifier: CA2465010091

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149501008G= , CM000685.2:g.149501008G=	GRCh38
NC_000023.10:g.148582539G= , CM000685.1:g.148582539G=	GRCh37
NC_000023.9:g.148390444G=	NCBI36
NG_011900.3:g.9327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.448C= MANE Select	ENSP00000339801.6:p.Pro150=
ENST00000651111.1:c.-186C=	ENSP00000498395.1:n.-186C=
ENST00000340855.10:c.448C=	ENSP00000339801.6:p.Pro150=
ENST00000370441.8:c.448C=	ENSP00000359470.4:p.Pro150=
ENST00000422081.6:c.-186C=	ENSP00000477056.1:n.-186C=
ENST00000441880.1:n.114-13910C=
ENST00000464251.5:c.374C=	ENSP00000428980.1:n.374C=
ENST00000466323.5:c.448C=	ENSP00000418264.1:p.Pro150=
ENST00000490775.5:n.107C=
ENST00000523759.5:n.562C=
NM_000202.6:c.448C=	NP_000193.1:p.Pro150=
NM_001166550.2:c.178C=	NP_001160022.1:p.Pro60=
NM_006123.4:c.448C=	NP_006114.1:p.Pro150=
NR_104128.1:n.665C=
NM_000202.7:c.448C=	NP_000193.1:p.Pro150=
NM_001166550.3:c.178C=	NP_001160022.1:p.Pro60=
NM_000202.8:c.448C= MANE Select	NP_000193.1:p.Pro150=
NM_001166550.4:c.178C=	NP_001160022.1:p.Pro60=
NM_006123.5:c.448C=	NP_006114.1:p.Pro150=
NR_104128.2:n.617C=