Canonical Allele Identifier: CA1947834849
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759613G= , CM000673.2:g.1759613G= GRCh38
NC_000011.9:g.1780843G= , CM000673.1:g.1780843G= GRCh37
NC_000011.8:g.1737419G= NCBI36
NG_008655.1:g.9380C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.255C= MANE Select ENSP00000236671.2:p.Ile85=
ENST00000367196.4:c.150C= ENSP00000356164.4:p.Ile50=
ENST00000429746.2:c.150C= ENSP00000402586.2:p.Ile50=
ENST00000433655.6:c.255C= ENSP00000404902.1:p.Ile85=
ENST00000438213.6:c.255C= ENSP00000415036.2:p.Ile85=
ENST00000636397.1:c.255C= ENSP00000489910.1:p.Ile85=
ENST00000636571.1:c.234C= ENSP00000490770.1:p.Ile78=
ENST00000636615.1:c.255C= ENSP00000490014.1:p.Ile85=
ENST00000636843.1:c.249C= ENSP00000490897.1:p.Ile83=
ENST00000637381.2:n.2683C=
ENST00000637387.1:c.255C= ENSP00000490598.1:p.Ile85=
ENST00000637815.2:c.255C= ENSP00000490344.1:p.Ile85=
ENST00000637915.1:c.255C= ENSP00000490471.1:p.Ile85=
ENST00000677300.1:n.650C=
ENST00000678991.1:c.*116C= ENSP00000503019.1:n.*116C=
ENST00000236671.6:c.255C= ENSP00000236671.2:p.Ile85=
ENST00000367196.3:c.150C= ENSP00000356164.3:p.Ile50=
ENST00000433655.5:c.255C= ENSP00000404902.1:p.Ile85=
ENST00000438213.5:c.210C= ENSP00000415036.1:p.Ile70=
NM_001909.4:c.255C= NP_001900.1:p.Ile85=
NM_001909.5:c.255C= MANE Select NP_001900.1:p.Ile85=