Canonical Allele Identifier: CA2838140039

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753484C>G , CM000673.2:g.1753484C>G	GRCh38
NC_000011.9:g.1774714C>G , CM000673.1:g.1774714C>G	GRCh37
NC_000011.8:g.1731290C>G	NCBI36
NG_008655.1:g.15509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*19G>C MANE Select	ENSP00000236671.2:n.*19G>C
ENST00000367196.4:c.*19G>C	ENSP00000356164.4:n.*19G>C
ENST00000427721.3:c.634+49G>C
ENST00000429746.2:c.*19G>C	ENSP00000402586.2:n.*19G>C
ENST00000433655.6:c.*424G>C	ENSP00000404902.1:n.*424G>C
ENST00000438213.6:c.*19G>C	ENSP00000415036.2:n.*19G>C
ENST00000636397.1:c.1071+319G>C	ENSP00000489910.1:n.1071+319G>C
ENST00000636571.1:c.*19G>C	ENSP00000490770.1:n.*19G>C
ENST00000636579.1:c.72+319G>C	ENSP00000490489.1:n.72+319G>C
ENST00000636615.1:c.1071+319G>C	ENSP00000490014.1:n.1071+319G>C
ENST00000636843.1:c.*19G>C	ENSP00000490897.1:n.*19G>C
ENST00000637158.1:n.856G>C
ENST00000637381.2:n.3686G>C
ENST00000637387.1:c.*19G>C	ENSP00000490598.1:n.*19G>C
ENST00000637815.2:c.*19G>C	ENSP00000490344.1:n.*19G>C
ENST00000637915.1:c.*19G>C	ENSP00000490471.1:n.*19G>C
ENST00000637937.1:n.566G>C
ENST00000678991.1:c.*1119G>C	ENSP00000503019.1:n.*1119G>C
ENST00000236671.6:c.*19G>C	ENSP00000236671.2:n.*19G>C
ENST00000427721.2:c.471+319G>C	ENSP00000415840.2:n.471+319G>C
ENST00000429746.1:c.589G>C	ENSP00000402586.1:n.589G>C
ENST00000433655.5:c.*424G>C	ENSP00000404902.1:n.*424G>C
NM_001909.4:c.*19G>C	NP_001900.1:n.*19G>C
NM_001909.5:c.*19G>C MANE Select	NP_001900.1:n.*19G>C