Canonical Allele Identifier: CA1947825056
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1753460G= , CM000673.2:g.1753460G= GRCh38
NC_000011.9:g.1774690G= , CM000673.1:g.1774690G= GRCh37
NC_000011.8:g.1731266G= NCBI36
NG_008655.1:g.15533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.*43C= MANE Select ENSP00000236671.2:n.*43C=
ENST00000367196.4:c.*43C= ENSP00000356164.4:n.*43C=
ENST00000427721.3:c.634+73C=
ENST00000429746.2:c.*43C= ENSP00000402586.2:n.*43C=
ENST00000433655.6:c.*448C= ENSP00000404902.1:n.*448C=
ENST00000438213.6:c.*43C= ENSP00000415036.2:n.*43C=
ENST00000636397.1:c.1071+343C= ENSP00000489910.1:n.1071+343C=
ENST00000636571.1:c.*43C= ENSP00000490770.1:n.*43C=
ENST00000636579.1:c.72+343C= ENSP00000490489.1:n.72+343C=
ENST00000636615.1:c.1071+343C= ENSP00000490014.1:n.1071+343C=
ENST00000636843.1:c.*43C= ENSP00000490897.1:n.*43C=
ENST00000637158.1:n.880C=
ENST00000637381.2:n.3710C=
ENST00000637387.1:c.*43C= ENSP00000490598.1:n.*43C=
ENST00000637815.2:c.*43C= ENSP00000490344.1:n.*43C=
ENST00000637915.1:c.*43C= ENSP00000490471.1:n.*43C=
ENST00000637937.1:n.590C=
ENST00000678991.1:c.*1143C= ENSP00000503019.1:n.*1143C=
ENST00000236671.6:c.*43C= ENSP00000236671.2:n.*43C=
ENST00000427721.2:c.471+343C= ENSP00000415840.2:n.471+343C=
ENST00000429746.1:c.613C= ENSP00000402586.1:n.613C=
ENST00000433655.5:c.*448C= ENSP00000404902.1:n.*448C=
NM_001909.4:c.*43C= NP_001900.1:n.*43C=
NM_001909.5:c.*43C= MANE Select NP_001900.1:n.*43C=