Canonical Allele Identifier: CA1947834726
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759574C= , CM000673.2:g.1759574C= GRCh38
NC_000011.9:g.1780804C= , CM000673.1:g.1780804C= GRCh37
NC_000011.8:g.1737380C= NCBI36
NG_008655.1:g.9419G=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.294G= MANE Select ENSP00000236671.2:p.Thr98=
ENST00000367196.4:c.189G= ENSP00000356164.4:p.Thr63=
ENST00000429746.2:c.189G= ENSP00000402586.2:p.Thr63=
ENST00000433655.6:c.294G= ENSP00000404902.1:p.Thr98=
ENST00000438213.6:c.294G= ENSP00000415036.2:p.Thr98=
ENST00000636397.1:c.294G= ENSP00000489910.1:p.Thr98=
ENST00000636571.1:c.273G= ENSP00000490770.1:p.Thr91=
ENST00000636615.1:c.294G= ENSP00000490014.1:p.Thr98=
ENST00000636843.1:c.288G= ENSP00000490897.1:p.Thr96=
ENST00000637381.2:n.2722G=
ENST00000637387.1:c.294G= ENSP00000490598.1:p.Thr98=
ENST00000637815.2:c.294G= ENSP00000490344.1:p.Thr98=
ENST00000637915.1:c.294G= ENSP00000490471.1:p.Thr98=
ENST00000677300.1:n.689G=
ENST00000678991.1:c.*155G= ENSP00000503019.1:n.*155G=
ENST00000236671.6:c.294G= ENSP00000236671.2:p.Thr98=
ENST00000367196.3:c.189G= ENSP00000356164.3:p.Thr63=
ENST00000433655.5:c.294G= ENSP00000404902.1:p.Thr98=
ENST00000438213.5:c.249G= ENSP00000415036.1:p.Thr83=
NM_001909.4:c.294G= NP_001900.1:p.Thr98=
NM_001909.5:c.294G= MANE Select NP_001900.1:p.Thr98=