Canonical Allele Identifier: CA1947834846
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759612C= , CM000673.2:g.1759612C= GRCh38
NC_000011.9:g.1780842C= , CM000673.1:g.1780842C= GRCh37
NC_000011.8:g.1737418C= NCBI36
NG_008655.1:g.9381G=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.256G= MANE Select ENSP00000236671.2:p.Gly86=
ENST00000367196.4:c.151G= ENSP00000356164.4:p.Gly51=
ENST00000429746.2:c.151G= ENSP00000402586.2:p.Gly51=
ENST00000433655.6:c.256G= ENSP00000404902.1:p.Gly86=
ENST00000438213.6:c.256G= ENSP00000415036.2:p.Gly86=
ENST00000636397.1:c.256G= ENSP00000489910.1:p.Gly86=
ENST00000636571.1:c.235G= ENSP00000490770.1:p.Gly79=
ENST00000636615.1:c.256G= ENSP00000490014.1:p.Gly86=
ENST00000636843.1:c.250G= ENSP00000490897.1:p.Gly84=
ENST00000637381.2:n.2684G=
ENST00000637387.1:c.256G= ENSP00000490598.1:p.Gly86=
ENST00000637815.2:c.256G= ENSP00000490344.1:p.Gly86=
ENST00000637915.1:c.256G= ENSP00000490471.1:p.Gly86=
ENST00000677300.1:n.651G=
ENST00000678991.1:c.*117G= ENSP00000503019.1:n.*117G=
ENST00000236671.6:c.256G= ENSP00000236671.2:p.Gly86=
ENST00000367196.3:c.151G= ENSP00000356164.3:p.Gly51=
ENST00000433655.5:c.256G= ENSP00000404902.1:p.Gly86=
ENST00000438213.5:c.211G= ENSP00000415036.1:p.Gly71=
NM_001909.4:c.256G= NP_001900.1:p.Gly86=
NM_001909.5:c.256G= MANE Select NP_001900.1:p.Gly86=