Canonical Allele Identifier: CA2694898452

Gene: IDS

Linked Data

• gnomAD v4: X-149501035-TCCCTTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149501036_149501042del , CM000685.2:g.149501036_149501042del	GRCh38
NC_000023.10:g.148582567_148582573del , CM000685.1:g.148582567_148582573del	GRCh37
NC_000023.9:g.148390472_148390478del	NCBI36
NG_011900.3:g.9293_9299del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.419-5_420del
ENST00000651111.1:c.-215-5_-214del
ENST00000340855.10:c.419-5_420del
ENST00000370441.8:c.419-5_420del
ENST00000422081.6:c.-215-5_-214del
ENST00000441880.1:n.114-13944_114-13938del
ENST00000464251.5:c.345-5_346del
ENST00000466323.5:c.419-5_420del
ENST00000490775.5:n.78-5_79del
ENST00000523759.5:n.533-5_534del
NM_000202.6:c.419-5_420del
NM_001166550.2:c.149-5_150del
NM_006123.4:c.419-5_420del
NR_104128.1:n.636-5_637del
NM_000202.7:c.419-5_420del
NM_001166550.3:c.149-5_150del
NM_000202.8:c.419-5_420del
NM_001166550.4:c.149-5_150del
NM_006123.5:c.419-5_420del
NR_104128.2:n.588-5_589del