Canonical Allele Identifier: CA414517869

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148564392T>A (hg19) ; chrX:g.149482861T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482861T>A , CM000685.2:g.149482861T>A	GRCh38
NC_000023.10:g.148564392T>A , CM000685.1:g.148564392T>A	GRCh37
NC_000023.9:g.148372297T>A	NCBI36
NG_011900.3:g.27474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1538A>T MANE Select	ENSP00000339801.6:p.Asn513Ile
ENST00000651111.1:c.905A>T	ENSP00000498395.1:p.Asn302Ile
ENST00000340855.10:c.1538A>T	ENSP00000339801.6:p.Asn513Ile
ENST00000422081.6:c.905A>T	ENSP00000477056.1:p.Asn302Ile
NM_000202.6:c.1538A>T	NP_000193.1:p.Asn513Ile
NM_001166550.2:c.1268A>T	NP_001160022.1:p.Asn423Ile
NM_000202.7:c.1538A>T	NP_000193.1:p.Asn513Ile
NM_001166550.3:c.1268A>T	NP_001160022.1:p.Asn423Ile
NM_000202.8:c.1538A>T MANE Select	NP_000193.1:p.Asn513Ile
NM_001166550.4:c.1268A>T	NP_001160022.1:p.Asn423Ile