Canonical Allele Identifier: CA1947825133
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1753605G= , CM000673.2:g.1753605G= GRCh38
NC_000011.9:g.1774835G= , CM000673.1:g.1774835G= GRCh37
NC_000011.8:g.1731411G= NCBI36
NG_008655.1:g.15388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.1137C= MANE Select ENSP00000236671.2:p.Ser379=
ENST00000367196.4:c.1032C= ENSP00000356164.4:p.Ser344=
ENST00000427721.3:c.562C=
ENST00000429746.2:c.1032C= ENSP00000402586.2:p.Ser344=
ENST00000433655.6:c.*303C= ENSP00000404902.1:n.*303C=
ENST00000438213.6:c.1254C= ENSP00000415036.2:p.Ser418=
ENST00000636397.1:c.1071+198C= ENSP00000489910.1:n.1071+198C=
ENST00000636571.1:c.1116C= ENSP00000490770.1:p.Ser372=
ENST00000636579.1:c.72+198C= ENSP00000490489.1:n.72+198C=
ENST00000636615.1:c.1071+198C= ENSP00000490014.1:n.1071+198C=
ENST00000636843.1:c.1131C= ENSP00000490897.1:p.Ser377=
ENST00000637158.1:n.735C=
ENST00000637381.2:n.3565C=
ENST00000637387.1:c.1116C= ENSP00000490598.1:p.Ser372=
ENST00000637815.2:c.1119C= ENSP00000490344.1:p.Ser373=
ENST00000637915.1:c.1128C= ENSP00000490471.1:p.Ser376=
ENST00000637937.1:n.445C=
ENST00000678991.1:c.*998C= ENSP00000503019.1:n.*998C=
ENST00000236671.6:c.1137C= ENSP00000236671.2:p.Ser379=
ENST00000427721.2:c.471+198C= ENSP00000415840.2:n.471+198C=
ENST00000429746.1:c.468C= ENSP00000402586.1:p.Ser156=
ENST00000433655.5:c.*303C= ENSP00000404902.1:n.*303C=
NM_001909.4:c.1137C= NP_001900.1:p.Ser379=
NM_001909.5:c.1137C= MANE Select NP_001900.1:p.Ser379=