Canonical Allele Identifier: CA2611926816

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753453-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753454del , CM000673.2:g.1753454del	GRCh38
NC_000011.9:g.1774684del , CM000673.1:g.1774684del	GRCh37
NC_000011.8:g.1731260del	NCBI36
NG_008655.1:g.15539del

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*49del MANE Select	ENSP00000236671.2:n.*49del
ENST00000367196.4:c.*49del	ENSP00000356164.4:n.*49del
ENST00000427721.3:c.634+79del
ENST00000429746.2:c.*49del	ENSP00000402586.2:n.*49del
ENST00000433655.6:c.*454del	ENSP00000404902.1:n.*454del
ENST00000438213.6:c.*49del	ENSP00000415036.2:n.*49del
ENST00000636397.1:c.1071+349del	ENSP00000489910.1:n.1071+349del
ENST00000636571.1:c.*49del	ENSP00000490770.1:n.*49del
ENST00000636579.1:c.72+349del	ENSP00000490489.1:n.72+349del
ENST00000636615.1:c.1071+349del	ENSP00000490014.1:n.1071+349del
ENST00000636843.1:c.*49del	ENSP00000490897.1:n.*49del
ENST00000637158.1:n.886del
ENST00000637381.2:n.3716del
ENST00000637387.1:c.*49del	ENSP00000490598.1:n.*49del
ENST00000637815.2:c.*49del	ENSP00000490344.1:n.*49del
ENST00000637915.1:c.*49del	ENSP00000490471.1:n.*49del
ENST00000637937.1:n.596del
ENST00000678991.1:c.*1149del	ENSP00000503019.1:n.*1149del
ENST00000236671.6:c.*49del	ENSP00000236671.2:n.*49del
ENST00000427721.2:c.471+349del	ENSP00000415840.2:n.471+349del
ENST00000429746.1:c.619del	ENSP00000402586.1:n.619del
ENST00000433655.5:c.*454del	ENSP00000404902.1:n.*454del
NM_001909.4:c.*49del	NP_001900.1:n.*49del
NM_001909.5:c.*49del MANE Select	NP_001900.1:n.*49del