Canonical Allele Identifier: CA1947825086
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1753508G= , CM000673.2:g.1753508G= GRCh38
NC_000011.9:g.1774738G= , CM000673.1:g.1774738G= GRCh37
NC_000011.8:g.1731314G= NCBI36
NG_008655.1:g.15485C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.1234C= MANE Select ENSP00000236671.2:p.Leu412=
ENST00000367196.4:c.1129C= ENSP00000356164.4:p.Leu377=
ENST00000427721.3:c.634+25C=
ENST00000429746.2:c.1129C= ENSP00000402586.2:p.Leu377=
ENST00000433655.6:c.*400C= ENSP00000404902.1:n.*400C=
ENST00000438213.6:c.1351C= ENSP00000415036.2:p.Leu451=
ENST00000636397.1:c.1071+295C= ENSP00000489910.1:n.1071+295C=
ENST00000636571.1:c.1213C= ENSP00000490770.1:p.Leu405=
ENST00000636579.1:c.72+295C= ENSP00000490489.1:n.72+295C=
ENST00000636615.1:c.1071+295C= ENSP00000490014.1:n.1071+295C=
ENST00000636843.1:c.1228C= ENSP00000490897.1:p.Leu410=
ENST00000637158.1:n.832C=
ENST00000637381.2:n.3662C=
ENST00000637387.1:c.1213C= ENSP00000490598.1:p.Leu405=
ENST00000637815.2:c.1216C= ENSP00000490344.1:p.Leu406=
ENST00000637915.1:c.1225C= ENSP00000490471.1:p.Leu409=
ENST00000637937.1:n.542C=
ENST00000678991.1:c.*1095C= ENSP00000503019.1:n.*1095C=
ENST00000236671.6:c.1234C= ENSP00000236671.2:p.Leu412=
ENST00000427721.2:c.471+295C= ENSP00000415840.2:n.471+295C=
ENST00000429746.1:c.565C= ENSP00000402586.1:p.Leu189=
ENST00000433655.5:c.*400C= ENSP00000404902.1:n.*400C=
NM_001909.4:c.1234C= NP_001900.1:p.Leu412=
NM_001909.5:c.1234C= MANE Select NP_001900.1:p.Leu412=