Canonical Allele Identifier: CA2465009239

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498225G= , CM000685.2:g.149498225G=	GRCh38
NC_000023.10:g.148579756G= , CM000685.1:g.148579756G=	GRCh37
NC_000023.9:g.148387661G=	NCBI36
NG_011900.3:g.12110C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.590C= MANE Select	ENSP00000339801.6:p.Pro197=
ENST00000651111.1:c.-44C=	ENSP00000498395.1:n.-44C=
ENST00000340855.10:c.590C=	ENSP00000339801.6:p.Pro197=
ENST00000370441.8:c.590C=	ENSP00000359470.4:p.Pro197=
ENST00000422081.6:c.-44C=	ENSP00000477056.1:n.-44C=
ENST00000441880.1:n.114-11127C=
ENST00000464251.5:c.516C=	ENSP00000428980.1:n.516C=
ENST00000466019.1:n.42C=
ENST00000466323.5:c.590C=	ENSP00000418264.1:p.Pro197=
ENST00000490775.5:n.375C=
ENST00000523759.5:n.704C=
NM_000202.6:c.590C=	NP_000193.1:p.Pro197=
NM_001166550.2:c.320C=	NP_001160022.1:p.Pro107=
NM_006123.4:c.590C=	NP_006114.1:p.Pro197=
NR_104128.1:n.807C=
NM_000202.7:c.590C=	NP_000193.1:p.Pro197=
NM_001166550.3:c.320C=	NP_001160022.1:p.Pro107=
NM_000202.8:c.590C= MANE Select	NP_000193.1:p.Pro197=
NM_001166550.4:c.320C=	NP_001160022.1:p.Pro107=
NM_006123.5:c.590C=	NP_006114.1:p.Pro197=
NR_104128.2:n.759C=