Canonical Allele Identifier: CA2465004120

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483318_149483319delinsCT , CM000685.2:g.149483318_149483319delinsCT	GRCh38
NC_000023.10:g.148564849_148564850delinsCT , CM000685.1:g.148564849_148564850delinsCT	GRCh37
NC_000023.9:g.148372754_148372755delinsCT	NCBI36
NG_011900.3:g.27016_27017delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1181-101_1181-100delinsAG MANE Select	ENSP00000339801.6:n.1181-101_1181-100delinsAG
ENST00000651111.1:c.548-101_548-100delinsAG	ENSP00000498395.1:n.548-101_548-100delinsAG
ENST00000340855.10:c.1181-101_1181-100delinsAG	ENSP00000339801.6:n.1181-101_1181-100delinsAG
ENST00000422081.6:c.548-101_548-100delinsAG	ENSP00000477056.1:n.548-101_548-100delinsAG
ENST00000441880.1:n.288-101_288-100delinsAG
NM_000202.6:c.1181-101_1181-100delinsAG	NP_000193.1:n.1181-101_1181-100delinsAG
NM_001166550.2:c.911-101_911-100delinsAG	NP_001160022.1:n.911-101_911-100delinsAG
NM_000202.7:c.1181-101_1181-100delinsAG	NP_000193.1:n.1181-101_1181-100delinsAG
NM_001166550.3:c.911-101_911-100delinsAG	NP_001160022.1:n.911-101_911-100delinsAG
NM_000202.8:c.1181-101_1181-100delinsAG MANE Select	NP_000193.1:n.1181-101_1181-100delinsAG
NM_001166550.4:c.911-101_911-100delinsAG	NP_001160022.1:n.911-101_911-100delinsAG