Canonical Allele Identifier: CA1947825139
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1753613G= , CM000673.2:g.1753613G= GRCh38
NC_000011.9:g.1774843G= , CM000673.1:g.1774843G= GRCh37
NC_000011.8:g.1731419G= NCBI36
NG_008655.1:g.15380C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.1129C= MANE Select ENSP00000236671.2:p.Pro377=
ENST00000367196.4:c.1024C= ENSP00000356164.4:p.Pro342=
ENST00000427721.3:c.554C=
ENST00000429746.2:c.1024C= ENSP00000402586.2:p.Pro342=
ENST00000433655.6:c.*295C= ENSP00000404902.1:n.*295C=
ENST00000438213.6:c.1246C= ENSP00000415036.2:p.Pro416=
ENST00000636397.1:c.1071+190C= ENSP00000489910.1:n.1071+190C=
ENST00000636571.1:c.1108C= ENSP00000490770.1:p.Pro370=
ENST00000636579.1:c.72+190C= ENSP00000490489.1:n.72+190C=
ENST00000636615.1:c.1071+190C= ENSP00000490014.1:n.1071+190C=
ENST00000636843.1:c.1123C= ENSP00000490897.1:p.Pro375=
ENST00000637158.1:n.727C=
ENST00000637381.2:n.3557C=
ENST00000637387.1:c.1108C= ENSP00000490598.1:p.Pro370=
ENST00000637815.2:c.1111C= ENSP00000490344.1:p.Pro371=
ENST00000637915.1:c.1120C= ENSP00000490471.1:p.Pro374=
ENST00000637937.1:n.437C=
ENST00000678991.1:c.*990C= ENSP00000503019.1:n.*990C=
ENST00000236671.6:c.1129C= ENSP00000236671.2:p.Pro377=
ENST00000427721.2:c.471+190C= ENSP00000415840.2:n.471+190C=
ENST00000429746.1:c.460C= ENSP00000402586.1:p.Pro154=
ENST00000433655.5:c.*295C= ENSP00000404902.1:n.*295C=
NM_001909.4:c.1129C= NP_001900.1:p.Pro377=
NM_001909.5:c.1129C= MANE Select NP_001900.1:p.Pro377=