Canonical Allele Identifier: CA2579719131

Gene: IDS

Linked Data

• gnomAD v4: X-149483313-G-GTTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483318_149483322dup , CM000685.2:g.149483318_149483322dup	GRCh38
NC_000023.10:g.148564849_148564853dup , CM000685.1:g.148564849_148564853dup	GRCh37
NC_000023.9:g.148372754_148372758dup	NCBI36
NG_011900.3:g.27017_27021dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-100_1181-96dup MANE Select	ENSP00000339801.6:n.1181-100_1181-96dup
ENST00000651111.1:c.548-100_548-96dup	ENSP00000498395.1:n.548-100_548-96dup
ENST00000340855.10:c.1181-100_1181-96dup	ENSP00000339801.6:n.1181-100_1181-96dup
ENST00000422081.6:c.548-100_548-96dup	ENSP00000477056.1:n.548-100_548-96dup
ENST00000441880.1:n.288-100_288-96dup
NM_000202.6:c.1181-100_1181-96dup	NP_000193.1:n.1181-100_1181-96dup
NM_001166550.2:c.911-100_911-96dup	NP_001160022.1:n.911-100_911-96dup
NM_000202.7:c.1181-100_1181-96dup	NP_000193.1:n.1181-100_1181-96dup
NM_001166550.3:c.911-100_911-96dup	NP_001160022.1:n.911-100_911-96dup
NM_000202.8:c.1181-100_1181-96dup MANE Select	NP_000193.1:n.1181-100_1181-96dup
NM_001166550.4:c.911-100_911-96dup	NP_001160022.1:n.911-100_911-96dup