Canonical Allele Identifier: CA2579719121

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483275_149483276insT , CM000685.2:g.149483275_149483276insT	GRCh38
NC_000023.10:g.148564806_148564807insT , CM000685.1:g.148564806_148564807insT	GRCh37
NC_000023.9:g.148372711_148372712insT	NCBI36
NG_011900.3:g.27059_27060insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-58_1181-57insA MANE Select	ENSP00000339801.6:n.1181-58_1181-57insA
ENST00000651111.1:c.548-58_548-57insA	ENSP00000498395.1:n.548-58_548-57insA
ENST00000340855.10:c.1181-58_1181-57insA	ENSP00000339801.6:n.1181-58_1181-57insA
ENST00000422081.6:c.548-58_548-57insA	ENSP00000477056.1:n.548-58_548-57insA
ENST00000441880.1:n.288-58_288-57insA
NM_000202.6:c.1181-58_1181-57insA	NP_000193.1:n.1181-58_1181-57insA
NM_001166550.2:c.911-58_911-57insA	NP_001160022.1:n.911-58_911-57insA
NM_000202.7:c.1181-58_1181-57insA	NP_000193.1:n.1181-58_1181-57insA
NM_001166550.3:c.911-58_911-57insA	NP_001160022.1:n.911-58_911-57insA
NM_000202.8:c.1181-58_1181-57insA MANE Select	NP_000193.1:n.1181-58_1181-57insA
NM_001166550.4:c.911-58_911-57insA	NP_001160022.1:n.911-58_911-57insA