Canonical Allele Identifier: CA519174209

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148564700C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483169C>A , CM000685.2:g.149483169C>A	GRCh38
NC_000023.10:g.148564700C>A , CM000685.1:g.148564700C>A	GRCh37
NC_000023.9:g.148372605C>A	NCBI36
NG_011900.3:g.27166G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1230G>T MANE Select	ENSP00000339801.6:p.Leu410=
ENST00000651111.1:c.597G>T	ENSP00000498395.1:p.Leu199=
ENST00000340855.10:c.1230G>T	ENSP00000339801.6:p.Leu410=
ENST00000422081.6:c.597G>T	ENSP00000477056.1:p.Leu199=
ENST00000441880.1:n.337G>T
NM_000202.6:c.1230G>T	NP_000193.1:p.Leu410=
NM_001166550.2:c.960G>T	NP_001160022.1:p.Leu320=
NM_000202.7:c.1230G>T	NP_000193.1:p.Leu410=
NM_001166550.3:c.960G>T	NP_001160022.1:p.Leu320=
NM_000202.8:c.1230G>T MANE Select	NP_000193.1:p.Leu410=
NM_001166550.4:c.960G>T	NP_001160022.1:p.Leu320=