Canonical Allele Identifier: CA2611926768

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753427-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753431dup , CM000673.2:g.1753431dup	GRCh38
NC_000011.9:g.1774661dup , CM000673.1:g.1774661dup	GRCh37
NC_000011.8:g.1731237dup	NCBI36
NG_008655.1:g.15565dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*75dup MANE Select	ENSP00000236671.2:n.*75dup
ENST00000367196.4:c.*75dup	ENSP00000356164.4:n.*75dup
ENST00000427721.3:c.634+105dup
ENST00000429746.2:c.*75dup	ENSP00000402586.2:n.*75dup
ENST00000433655.6:c.*480dup	ENSP00000404902.1:n.*480dup
ENST00000438213.6:c.*75dup	ENSP00000415036.2:n.*75dup
ENST00000636397.1:c.1071+375dup	ENSP00000489910.1:n.1071+375dup
ENST00000636571.1:c.*75dup	ENSP00000490770.1:n.*75dup
ENST00000636579.1:c.72+375dup	ENSP00000490489.1:n.72+375dup
ENST00000636615.1:c.1071+375dup	ENSP00000490014.1:n.1071+375dup
ENST00000636843.1:c.*75dup	ENSP00000490897.1:n.*75dup
ENST00000637158.1:n.912dup
ENST00000637381.2:n.3742dup
ENST00000637387.1:c.*75dup	ENSP00000490598.1:n.*75dup
ENST00000637815.2:c.*75dup	ENSP00000490344.1:n.*75dup
ENST00000637915.1:c.*75dup	ENSP00000490471.1:n.*75dup
ENST00000637937.1:n.622dup
ENST00000678991.1:c.*1175dup	ENSP00000503019.1:n.*1175dup
ENST00000236671.6:c.*75dup	ENSP00000236671.2:n.*75dup
ENST00000427721.2:c.471+375dup	ENSP00000415840.2:n.471+375dup
ENST00000429746.1:c.645dup	ENSP00000402586.1:n.645dup
ENST00000433655.5:c.*480dup	ENSP00000404902.1:n.*480dup
NM_001909.4:c.*75dup	NP_001900.1:n.*75dup
NM_001909.5:c.*75dup MANE Select	NP_001900.1:n.*75dup