Canonical Allele Identifier: CA2465005623

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487152_149487156delinsCTTGT , CM000685.2:g.149487152_149487156delinsCTTGT	GRCh38
NC_000023.10:g.148568683_148568687delinsCTTGT , CM000685.1:g.148568683_148568687delinsCTTGT	GRCh37
NC_000023.9:g.148376588_148376592delinsCTTGT	NCBI36
NG_011900.3:g.23179_23183delinsACAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-58_1007-54delinsACAAG MANE Select	ENSP00000339801.6:n.1007-58_1007-54delinsACAAG
ENST00000651111.1:c.374-58_374-54delinsACAAG	ENSP00000498395.1:n.374-58_374-54delinsACAAG
ENST00000340855.10:c.1007-58_1007-54delinsACAAG	ENSP00000339801.6:n.1007-58_1007-54delinsACAAG
ENST00000370441.8:c.*132_*136delinsACAAG	ENSP00000359470.4:n.*132_*136delinsACAAG
ENST00000422081.6:c.374-58_374-54delinsACAAG	ENSP00000477056.1:n.374-58_374-54delinsACAAG
ENST00000441880.1:n.114-58_114-54delinsACAAG
ENST00000466323.5:c.*355_*359delinsACAAG	ENSP00000418264.1:n.*355_*359delinsACAAG
NM_000202.6:c.1007-58_1007-54delinsACAAG	NP_000193.1:n.1007-58_1007-54delinsACAAG
NM_001166550.2:c.737-58_737-54delinsACAAG	NP_001160022.1:n.737-58_737-54delinsACAAG
NM_006123.4:c.*132_*136delinsACAAG	NP_006114.1:n.*132_*136delinsACAAG
NR_104128.1:n.1511_1515delinsACAAG
NM_000202.7:c.1007-58_1007-54delinsACAAG	NP_000193.1:n.1007-58_1007-54delinsACAAG
NM_001166550.3:c.737-58_737-54delinsACAAG	NP_001160022.1:n.737-58_737-54delinsACAAG
NM_000202.8:c.1007-58_1007-54delinsACAAG MANE Select	NP_000193.1:n.1007-58_1007-54delinsACAAG
NM_001166550.4:c.737-58_737-54delinsACAAG	NP_001160022.1:n.737-58_737-54delinsACAAG
NM_006123.5:c.*132_*136delinsACAAG	NP_006114.1:n.*132_*136delinsACAAG
NR_104128.2:n.1463_1467delinsACAAG