Canonical Allele Identifier: CA2694898121

Gene: IDS

Linked Data

• gnomAD v4: X-149498064-GCTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498066_149498069del , CM000685.2:g.149498066_149498069del	GRCh38
NC_000023.10:g.148579597_148579600del , CM000685.1:g.148579597_148579600del	GRCh37
NC_000023.9:g.148387502_148387505del	NCBI36
NG_011900.3:g.12267_12270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.708+39_708+42del MANE Select	ENSP00000339801.6:n.708+39_708+42del
ENST00000651111.1:c.75+39_75+42del	ENSP00000498395.1:n.75+39_75+42del
ENST00000340855.10:c.708+39_708+42del	ENSP00000339801.6:n.708+39_708+42del
ENST00000370441.8:c.708+39_708+42del	ENSP00000359470.4:n.708+39_708+42del
ENST00000422081.6:c.75+39_75+42del	ENSP00000477056.1:n.75+39_75+42del
ENST00000441880.1:n.114-10970_114-10967del
ENST00000464251.5:c.634+39_634+42del	ENSP00000428980.1:n.634+39_634+42del
ENST00000466019.1:n.160+39_160+42del
ENST00000466323.5:c.708+39_708+42del	ENSP00000418264.1:n.708+39_708+42del
ENST00000490775.5:n.493+39_493+42del
NM_000202.6:c.708+39_708+42del	NP_000193.1:n.708+39_708+42del
NM_001166550.2:c.438+39_438+42del	NP_001160022.1:n.438+39_438+42del
NM_006123.4:c.708+39_708+42del	NP_006114.1:n.708+39_708+42del
NR_104128.1:n.925+39_925+42del
NM_000202.7:c.708+39_708+42del	NP_000193.1:n.708+39_708+42del
NM_001166550.3:c.438+39_438+42del	NP_001160022.1:n.438+39_438+42del
NM_000202.8:c.708+39_708+42del MANE Select	NP_000193.1:n.708+39_708+42del
NM_001166550.4:c.438+39_438+42del	NP_001160022.1:n.438+39_438+42del
NM_006123.5:c.708+39_708+42del	NP_006114.1:n.708+39_708+42del
NR_104128.2:n.877+39_877+42del