Canonical Allele Identifier: CA1947826314
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1754975T= , CM000673.2:g.1754975T= GRCh38
NC_000011.9:g.1776205T= , CM000673.1:g.1776205T= GRCh37
NC_000011.8:g.1732781T= NCBI36
NG_008655.1:g.14018A=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.758A= MANE Select ENSP00000236671.2:p.Lys253=
ENST00000367196.4:c.653A= ENSP00000356164.4:p.Lys218=
ENST00000427721.3:c.183A=
ENST00000429746.2:c.653A= ENSP00000402586.2:p.Lys218=
ENST00000433655.6:c.758A= ENSP00000404902.1:p.Lys253=
ENST00000438213.6:c.758A= ENSP00000415036.2:p.Lys253=
ENST00000497544.3:n.374A=
ENST00000636397.1:c.758A= ENSP00000489910.1:p.Lys253=
ENST00000636571.1:c.737A= ENSP00000490770.1:p.Lys246=
ENST00000636615.1:c.758A= ENSP00000490014.1:p.Lys253=
ENST00000636843.1:c.752A= ENSP00000490897.1:p.Lys251=
ENST00000637158.1:n.356A=
ENST00000637381.2:n.3186A=
ENST00000637387.1:c.758A= ENSP00000490598.1:p.Lys253=
ENST00000637815.2:c.758A= ENSP00000490344.1:p.Lys253=
ENST00000637915.1:c.758A= ENSP00000490471.1:p.Lys253=
ENST00000637937.1:n.66A=
ENST00000678991.1:c.*619A= ENSP00000503019.1:n.*619A=
ENST00000236671.6:c.758A= ENSP00000236671.2:p.Lys253=
ENST00000427721.2:c.158A= ENSP00000415840.2:p.Lys53=
ENST00000433655.5:c.758A= ENSP00000404902.1:p.Lys253=
ENST00000438213.5:c.713A= ENSP00000415036.1:p.Lys238=
ENST00000497544.1:n.374A=
NM_001909.4:c.758A= NP_001900.1:p.Lys253=
NM_001909.5:c.758A= MANE Select NP_001900.1:p.Lys253=