Canonical Allele Identifier: CA519058454

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579836T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498305T>A , CM000685.2:g.149498305T>A	GRCh38
NC_000023.10:g.148579836T>A , CM000685.1:g.148579836T>A	GRCh37
NC_000023.9:g.148387741T>A	NCBI36
NG_011900.3:g.12030A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.510A>T MANE Select	ENSP00000339801.6:p.Thr170=
ENST00000651111.1:c.-124A>T	ENSP00000498395.1:n.-124A>T
ENST00000340855.10:c.510A>T	ENSP00000339801.6:p.Thr170=
ENST00000370441.8:c.510A>T	ENSP00000359470.4:p.Thr170=
ENST00000422081.6:c.-124A>T	ENSP00000477056.1:n.-124A>T
ENST00000441880.1:n.114-11207A>T
ENST00000464251.5:c.436A>T	ENSP00000428980.1:n.436A>T
ENST00000466323.5:c.510A>T	ENSP00000418264.1:p.Thr170=
ENST00000490775.5:n.295A>T
ENST00000523759.5:n.624A>T
NM_000202.6:c.510A>T	NP_000193.1:p.Thr170=
NM_001166550.2:c.240A>T	NP_001160022.1:p.Thr80=
NM_006123.4:c.510A>T	NP_006114.1:p.Thr170=
NR_104128.1:n.727A>T
NM_000202.7:c.510A>T	NP_000193.1:p.Thr170=
NM_001166550.3:c.240A>T	NP_001160022.1:p.Thr80=
NM_000202.8:c.510A>T MANE Select	NP_000193.1:p.Thr170=
NM_001166550.4:c.240A>T	NP_001160022.1:p.Thr80=
NM_006123.5:c.510A>T	NP_006114.1:p.Thr170=
NR_104128.2:n.679A>T