Canonical Allele Identifier: CA1947834648
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759523G= , CM000673.2:g.1759523G= GRCh38
NC_000011.9:g.1780753G= , CM000673.1:g.1780753G= GRCh37
NC_000011.8:g.1737329G= NCBI36
NG_008655.1:g.9470C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.345C= MANE Select ENSP00000236671.2:p.Ile115=
ENST00000367196.4:c.240C= ENSP00000356164.4:p.Ile80=
ENST00000429746.2:c.240C= ENSP00000402586.2:p.Ile80=
ENST00000433655.6:c.345C= ENSP00000404902.1:p.Ile115=
ENST00000438213.6:c.345C= ENSP00000415036.2:p.Ile115=
ENST00000636397.1:c.345C= ENSP00000489910.1:p.Ile115=
ENST00000636571.1:c.324C= ENSP00000490770.1:p.Ile108=
ENST00000636615.1:c.345C= ENSP00000490014.1:p.Ile115=
ENST00000636843.1:c.339C= ENSP00000490897.1:p.Ile113=
ENST00000637381.2:n.2773C=
ENST00000637387.1:c.345C= ENSP00000490598.1:p.Ile115=
ENST00000637815.2:c.345C= ENSP00000490344.1:p.Ile115=
ENST00000637915.1:c.345C= ENSP00000490471.1:p.Ile115=
ENST00000677300.1:n.740C=
ENST00000678991.1:c.*206C= ENSP00000503019.1:n.*206C=
ENST00000236671.6:c.345C= ENSP00000236671.2:p.Ile115=
ENST00000367196.3:c.240C= ENSP00000356164.3:p.Ile80=
ENST00000433655.5:c.345C= ENSP00000404902.1:p.Ile115=
ENST00000438213.5:c.300C= ENSP00000415036.1:p.Ile100=
NM_001909.4:c.345C= NP_001900.1:p.Ile115=
NM_001909.5:c.345C= MANE Select NP_001900.1:p.Ile115=