Canonical Allele Identifier: CA2694898005

Gene: IDS

Linked Data

• gnomAD v4: X-149496552-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496555_149496556del , CM000685.2:g.149496555_149496556del	GRCh38
NC_000023.10:g.148578086_148578087del , CM000685.1:g.148578086_148578087del	GRCh37
NC_000023.9:g.148385991_148385992del	NCBI36
NG_011900.3:g.13781_13782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-38_709-37del MANE Select	ENSP00000339801.6:n.709-38_709-37del
ENST00000651111.1:c.76-38_76-37del	ENSP00000498395.1:n.76-38_76-37del
ENST00000340855.10:c.709-38_709-37del	ENSP00000339801.6:n.709-38_709-37del
ENST00000370441.8:c.709-38_709-37del	ENSP00000359470.4:n.709-38_709-37del
ENST00000422081.6:c.76-38_76-37del	ENSP00000477056.1:n.76-38_76-37del
ENST00000441880.1:n.114-9456_114-9455del
ENST00000464251.5:c.635-38_635-37del	ENSP00000428980.1:n.635-38_635-37del
ENST00000466019.1:n.161-38_161-37del
ENST00000466323.5:c.709-38_709-37del	ENSP00000418264.1:n.709-38_709-37del
ENST00000490775.5:n.494-38_494-37del
NM_000202.6:c.709-38_709-37del	NP_000193.1:n.709-38_709-37del
NM_001166550.2:c.439-38_439-37del	NP_001160022.1:n.439-38_439-37del
NM_006123.4:c.709-38_709-37del	NP_006114.1:n.709-38_709-37del
NR_104128.1:n.926-38_926-37del
NM_000202.7:c.709-38_709-37del	NP_000193.1:n.709-38_709-37del
NM_001166550.3:c.439-38_439-37del	NP_001160022.1:n.439-38_439-37del
NM_000202.8:c.709-38_709-37del MANE Select	NP_000193.1:n.709-38_709-37del
NM_001166550.4:c.439-38_439-37del	NP_001160022.1:n.439-38_439-37del
NM_006123.5:c.709-38_709-37del	NP_006114.1:n.709-38_709-37del
NR_104128.2:n.878-38_878-37del