Canonical Allele Identifier: CA1947825390
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1754026C= , CM000673.2:g.1754026C= GRCh38
NC_000011.9:g.1775256C= , CM000673.1:g.1775256C= GRCh37
NC_000011.8:g.1731832C= NCBI36
NG_008655.1:g.14967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000236671.7:c.940G= MANE Select ENSP00000236671.2:p.Ala314=
ENST00000367196.4:c.835G= ENSP00000356164.4:p.Ala279=
ENST00000427721.3:c.365G=
ENST00000429746.2:c.835G= ENSP00000402586.2:p.Ala279=
ENST00000433655.6:c.*106G= ENSP00000404902.1:n.*106G=
ENST00000438213.6:c.1057G= ENSP00000415036.2:p.Ala353=
ENST00000497544.3:n.556G=
ENST00000636397.1:c.940G= ENSP00000489910.1:p.Ala314=
ENST00000636571.1:c.919G= ENSP00000490770.1:p.Ala307=
ENST00000636615.1:c.940G= ENSP00000490014.1:p.Ala314=
ENST00000636843.1:c.934G= ENSP00000490897.1:p.Ala312=
ENST00000637158.1:n.538G=
ENST00000637381.2:n.3368G=
ENST00000637387.1:c.940G= ENSP00000490598.1:p.Ala314=
ENST00000637815.2:c.922G= ENSP00000490344.1:p.Ala308=
ENST00000637915.1:c.940G= ENSP00000490471.1:p.Ala314=
ENST00000637937.1:n.248G=
ENST00000678991.1:c.*801G= ENSP00000503019.1:n.*801G=
ENST00000236671.6:c.940G= ENSP00000236671.2:p.Ala314=
ENST00000427721.2:c.340G= ENSP00000415840.2:p.Ala114=
ENST00000429746.1:c.271G= ENSP00000402586.1:p.Ala91=
ENST00000433655.5:c.*106G= ENSP00000404902.1:n.*106G=
ENST00000438213.5:c.895G= ENSP00000415036.1:p.Ala299=
ENST00000497544.1:n.556G=
NM_001909.4:c.940G= NP_001900.1:p.Ala314=
NM_001909.5:c.940G= MANE Select NP_001900.1:p.Ala314=