Canonical Allele Identifier: CA1947834760
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759582A= , CM000673.2:g.1759582A= GRCh38
NC_000011.9:g.1780812A= , CM000673.1:g.1780812A= GRCh37
NC_000011.8:g.1737388A= NCBI36
NG_008655.1:g.9411T=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.286T= MANE Select ENSP00000236671.2:p.Phe96=
ENST00000367196.4:c.181T= ENSP00000356164.4:p.Phe61=
ENST00000429746.2:c.181T= ENSP00000402586.2:p.Phe61=
ENST00000433655.6:c.286T= ENSP00000404902.1:p.Phe96=
ENST00000438213.6:c.286T= ENSP00000415036.2:p.Phe96=
ENST00000636397.1:c.286T= ENSP00000489910.1:p.Phe96=
ENST00000636571.1:c.265T= ENSP00000490770.1:p.Phe89=
ENST00000636615.1:c.286T= ENSP00000490014.1:p.Phe96=
ENST00000636843.1:c.280T= ENSP00000490897.1:p.Phe94=
ENST00000637381.2:n.2714T=
ENST00000637387.1:c.286T= ENSP00000490598.1:p.Phe96=
ENST00000637815.2:c.286T= ENSP00000490344.1:p.Phe96=
ENST00000637915.1:c.286T= ENSP00000490471.1:p.Phe96=
ENST00000677300.1:n.681T=
ENST00000678991.1:c.*147T= ENSP00000503019.1:n.*147T=
ENST00000236671.6:c.286T= ENSP00000236671.2:p.Phe96=
ENST00000367196.3:c.181T= ENSP00000356164.3:p.Phe61=
ENST00000433655.5:c.286T= ENSP00000404902.1:p.Phe96=
ENST00000438213.5:c.241T= ENSP00000415036.1:p.Phe81=
NM_001909.4:c.286T= NP_001900.1:p.Phe96=
NM_001909.5:c.286T= MANE Select NP_001900.1:p.Phe96=