Canonical Allele Identifier: CA2824136136

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487116C>T , CM000685.2:g.149487116C>T	GRCh38
NC_000023.10:g.148568647C>T , CM000685.1:g.148568647C>T	GRCh37
NC_000023.9:g.148376552C>T	NCBI36
NG_011900.3:g.23219G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-18G>A MANE Select	ENSP00000339801.6:n.1007-18G>A
ENST00000651111.1:c.374-18G>A	ENSP00000498395.1:n.374-18G>A
ENST00000340855.10:c.1007-18G>A	ENSP00000339801.6:n.1007-18G>A
ENST00000422081.6:c.374-18G>A	ENSP00000477056.1:n.374-18G>A
ENST00000441880.1:n.114-18G>A
NM_000202.6:c.1007-18G>A	NP_000193.1:n.1007-18G>A
NM_001166550.2:c.737-18G>A	NP_001160022.1:n.737-18G>A
NM_000202.7:c.1007-18G>A	NP_000193.1:n.1007-18G>A
NM_001166550.3:c.737-18G>A	NP_001160022.1:n.737-18G>A
NM_000202.8:c.1007-18G>A MANE Select	NP_000193.1:n.1007-18G>A
NM_001166550.4:c.737-18G>A	NP_001160022.1:n.737-18G>A