Canonical Allele Identifier: CA2694908959

Gene: IDS

Linked Data

• gnomAD v4: X-149483233-G-GACAGAGCAGAATGGGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483237_149483253dup , CM000685.2:g.149483237_149483253dup	GRCh38
NC_000023.10:g.148564768_148564784dup , CM000685.1:g.148564768_148564784dup	GRCh37
NC_000023.9:g.148372673_148372689dup	NCBI36
NG_011900.3:g.27085_27101dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-32_1181-16dup MANE Select	ENSP00000339801.6:n.1181-32_1181-16dup
ENST00000651111.1:c.548-32_548-16dup	ENSP00000498395.1:n.548-32_548-16dup
ENST00000340855.10:c.1181-32_1181-16dup	ENSP00000339801.6:n.1181-32_1181-16dup
ENST00000422081.6:c.548-32_548-16dup	ENSP00000477056.1:n.548-32_548-16dup
ENST00000441880.1:n.288-32_288-16dup
NM_000202.6:c.1181-32_1181-16dup	NP_000193.1:n.1181-32_1181-16dup
NM_001166550.2:c.911-32_911-16dup	NP_001160022.1:n.911-32_911-16dup
NM_000202.7:c.1181-32_1181-16dup	NP_000193.1:n.1181-32_1181-16dup
NM_001166550.3:c.911-32_911-16dup	NP_001160022.1:n.911-32_911-16dup
NM_000202.8:c.1181-32_1181-16dup MANE Select	NP_000193.1:n.1181-32_1181-16dup
NM_001166550.4:c.911-32_911-16dup	NP_001160022.1:n.911-32_911-16dup