Canonical Allele Identifier: CA414518297

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148564589C>A (hg19) ; chrX:g.149483058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483058C>A , CM000685.2:g.149483058C>A	GRCh38
NC_000023.10:g.148564589C>A , CM000685.1:g.148564589C>A	GRCh37
NC_000023.9:g.148372494C>A	NCBI36
NG_011900.3:g.27277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1341G>T MANE Select	ENSP00000339801.6:p.Leu447Phe
ENST00000651111.1:c.708G>T	ENSP00000498395.1:p.Leu236Phe
ENST00000340855.10:c.1341G>T	ENSP00000339801.6:p.Leu447Phe
ENST00000422081.6:c.708G>T	ENSP00000477056.1:p.Leu236Phe
NM_000202.6:c.1341G>T	NP_000193.1:p.Leu447Phe
NM_001166550.2:c.1071G>T	NP_001160022.1:p.Leu357Phe
NM_000202.7:c.1341G>T	NP_000193.1:p.Leu447Phe
NM_001166550.3:c.1071G>T	NP_001160022.1:p.Leu357Phe
NM_000202.8:c.1341G>T MANE Select	NP_000193.1:p.Leu447Phe
NM_001166550.4:c.1071G>T	NP_001160022.1:p.Leu357Phe