Canonical Allele Identifier: CA1947834824
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759606G= , CM000673.2:g.1759606G= GRCh38
NC_000011.9:g.1780836G= , CM000673.1:g.1780836G= GRCh37
NC_000011.8:g.1737412G= NCBI36
NG_008655.1:g.9387C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.262C= MANE Select ENSP00000236671.2:p.Pro88=
ENST00000367196.4:c.157C= ENSP00000356164.4:p.Pro53=
ENST00000429746.2:c.157C= ENSP00000402586.2:p.Pro53=
ENST00000433655.6:c.262C= ENSP00000404902.1:p.Pro88=
ENST00000438213.6:c.262C= ENSP00000415036.2:p.Pro88=
ENST00000636397.1:c.262C= ENSP00000489910.1:p.Pro88=
ENST00000636571.1:c.241C= ENSP00000490770.1:p.Pro81=
ENST00000636615.1:c.262C= ENSP00000490014.1:p.Pro88=
ENST00000636843.1:c.256C= ENSP00000490897.1:p.Pro86=
ENST00000637381.2:n.2690C=
ENST00000637387.1:c.262C= ENSP00000490598.1:p.Pro88=
ENST00000637815.2:c.262C= ENSP00000490344.1:p.Pro88=
ENST00000637915.1:c.262C= ENSP00000490471.1:p.Pro88=
ENST00000677300.1:n.657C=
ENST00000678991.1:c.*123C= ENSP00000503019.1:n.*123C=
ENST00000236671.6:c.262C= ENSP00000236671.2:p.Pro88=
ENST00000367196.3:c.157C= ENSP00000356164.3:p.Pro53=
ENST00000433655.5:c.262C= ENSP00000404902.1:p.Pro88=
ENST00000438213.5:c.217C= ENSP00000415036.1:p.Pro73=
NM_001909.4:c.262C= NP_001900.1:p.Pro88=
NM_001909.5:c.262C= MANE Select NP_001900.1:p.Pro88=