Canonical Allele Identifier: CA1947834632
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1759508T= , CM000673.2:g.1759508T= GRCh38
NC_000011.9:g.1780738T= , CM000673.1:g.1780738T= GRCh37
NC_000011.8:g.1737314T= NCBI36
NG_008655.1:g.9485A=

Transcript Alleles

HGVS Amino-acid change
ENST00000236671.7:c.352+8A= MANE Select ENSP00000236671.2:n.352+8A=
ENST00000367196.4:c.247+8A= ENSP00000356164.4:n.247+8A=
ENST00000429746.2:c.247+8A= ENSP00000402586.2:n.247+8A=
ENST00000433655.6:c.352+8A= ENSP00000404902.1:n.352+8A=
ENST00000438213.6:c.352+8A= ENSP00000415036.2:n.352+8A=
ENST00000636397.1:c.352+8A= ENSP00000489910.1:n.352+8A=
ENST00000636571.1:c.331+8A= ENSP00000490770.1:n.331+8A=
ENST00000636615.1:c.352+8A= ENSP00000490014.1:n.352+8A=
ENST00000636843.1:c.346+8A= ENSP00000490897.1:n.346+8A=
ENST00000637381.2:n.2780+8A=
ENST00000637387.1:c.352+8A= ENSP00000490598.1:n.352+8A=
ENST00000637815.2:c.352+8A= ENSP00000490344.1:n.352+8A=
ENST00000637915.1:c.352+8A= ENSP00000490471.1:n.352+8A=
ENST00000677300.1:n.747+8A=
ENST00000678991.1:c.*213+8A= ENSP00000503019.1:n.*213+8A=
ENST00000236671.6:c.352+8A= ENSP00000236671.2:n.352+8A=
ENST00000367196.3:c.247+8A= ENSP00000356164.3:n.247+8A=
ENST00000433655.5:c.352+8A= ENSP00000404902.1:n.352+8A=
ENST00000438213.5:c.307+8A= ENSP00000415036.1:n.307+8A=
NM_001909.4:c.352+8A= NP_001900.1:n.352+8A=
NM_001909.5:c.352+8A= MANE Select NP_001900.1:n.352+8A=