Canonical Allele Identifier: CA2579719279

Gene: IDS

Linked Data

• gnomAD v4: X-149500887-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149500887G>T , CM000685.2:g.149500887G>T	GRCh38
NC_000023.10:g.148582418G>T , CM000685.1:g.148582418G>T	GRCh37
NC_000023.9:g.148390323G>T	NCBI36
NG_011900.3:g.9448C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.507+62C>A MANE Select	ENSP00000339801.6:n.507+62C>A
ENST00000651111.1:c.-127+62C>A	ENSP00000498395.1:n.-127+62C>A
ENST00000340855.10:c.507+62C>A	ENSP00000339801.6:n.507+62C>A
ENST00000370441.8:c.507+62C>A	ENSP00000359470.4:n.507+62C>A
ENST00000422081.6:c.-127+62C>A	ENSP00000477056.1:n.-127+62C>A
ENST00000441880.1:n.114-13789C>A
ENST00000464251.5:c.433+62C>A	ENSP00000428980.1:n.433+62C>A
ENST00000466323.5:c.507+62C>A	ENSP00000418264.1:n.507+62C>A
ENST00000490775.5:n.166+62C>A
ENST00000523759.5:n.621+62C>A
NM_000202.6:c.507+62C>A	NP_000193.1:n.507+62C>A
NM_001166550.2:c.237+62C>A	NP_001160022.1:n.237+62C>A
NM_006123.4:c.507+62C>A	NP_006114.1:n.507+62C>A
NR_104128.1:n.724+62C>A
NM_000202.7:c.507+62C>A	NP_000193.1:n.507+62C>A
NM_001166550.3:c.237+62C>A	NP_001160022.1:n.237+62C>A
NM_000202.8:c.507+62C>A MANE Select	NP_000193.1:n.507+62C>A
NM_001166550.4:c.237+62C>A	NP_001160022.1:n.237+62C>A
NM_006123.5:c.507+62C>A	NP_006114.1:n.507+62C>A
NR_104128.2:n.676+62C>A