Canonical Allele Identifier: CA2695236586

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503378_149503380del , CM000685.2:g.149503378_149503380del	GRCh38
NC_000023.10:g.148584908_148584910del , CM000685.1:g.148584908_148584910del	GRCh37
NC_000023.9:g.148392813_148392815del	NCBI36
NG_011900.3:g.6958_6960del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.353_355del MANE Select	ENSP00000339801.6:p.Thr118del
ENST00000651111.1:c.-215-2340_-215-2338del	ENSP00000498395.1:n.-215-2340_-215-2338de...
ENST00000340855.10:c.353_355del	ENSP00000339801.6:p.Thr118del
ENST00000370441.8:c.353_355del	ENSP00000359470.4:p.Thr118del
ENST00000422081.6:c.-215-2340_-215-2338del	ENSP00000477056.1:n.-215-2340_-215-2338de...
ENST00000427113.2:n.770-1154_770-1152del
ENST00000428056.6:c.353_355del	ENSP00000390241.2:p.Thr118del
ENST00000441880.1:n.114-16279_114-16277del
ENST00000464251.5:c.176_178del	ENSP00000428980.1:p.Thr59del
ENST00000466323.5:c.353_355del	ENSP00000418264.1:p.Thr118del
ENST00000490775.5:n.12_14del
ENST00000523759.5:n.533-2340_533-2338del
NM_000202.6:c.353_355del	NP_000193.1:p.Thr118del
NM_001166550.2:c.83_85del	NP_001160022.1:p.Thr28del
NM_006123.4:c.353_355del	NP_006114.1:p.Thr118del
NR_104128.1:n.570_572del
NM_000202.7:c.353_355del	NP_000193.1:p.Thr118del
NM_001166550.3:c.83_85del	NP_001160022.1:p.Thr28del
NM_000202.8:c.353_355del MANE Select	NP_000193.1:p.Thr118del
NM_001166550.4:c.83_85del	NP_001160022.1:p.Thr28del
NM_006123.5:c.353_355del	NP_006114.1:p.Thr118del
NR_104128.2:n.522_524del