Canonical Allele Identifier: CA1947825365

Gene: CTSD

Linked Data

• ClinVar Variation Id: 2756581
• ClinVar RCV Id: RCV003531833
• dbSNP Id: rs913538989

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753981C>T , CM000673.2:g.1753981C>T	GRCh38
NC_000011.9:g.1775211C>T , CM000673.1:g.1775211C>T	GRCh37
NC_000011.8:g.1731787C>T	NCBI36
NG_008655.1:g.15012G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.972+13G>A MANE Select	ENSP00000236671.2:n.972+13G>A
ENST00000367196.4:c.867+13G>A	ENSP00000356164.4:n.867+13G>A
ENST00000427721.3:c.397+13G>A
ENST00000429746.2:c.867+13G>A	ENSP00000402586.2:n.867+13G>A
ENST00000433655.6:c.*138+13G>A	ENSP00000404902.1:n.*138+13G>A
ENST00000438213.6:c.1089+13G>A	ENSP00000415036.2:n.1089+13G>A
ENST00000497544.3:n.601G>A
ENST00000636397.1:c.972+13G>A	ENSP00000489910.1:n.972+13G>A
ENST00000636571.1:c.951+13G>A	ENSP00000490770.1:n.951+13G>A
ENST00000636615.1:c.972+13G>A	ENSP00000490014.1:n.972+13G>A
ENST00000636843.1:c.966+13G>A	ENSP00000490897.1:n.966+13G>A
ENST00000637158.1:n.570+13G>A
ENST00000637381.2:n.3400+13G>A
ENST00000637387.1:c.972+13G>A	ENSP00000490598.1:n.972+13G>A
ENST00000637815.2:c.954+13G>A	ENSP00000490344.1:n.954+13G>A
ENST00000637915.1:c.972+13G>A	ENSP00000490471.1:n.972+13G>A
ENST00000637937.1:n.280+13G>A
ENST00000678991.1:c.*833+13G>A	ENSP00000503019.1:n.*833+13G>A
ENST00000236671.6:c.972+13G>A	ENSP00000236671.2:n.972+13G>A
ENST00000427721.2:c.372+13G>A	ENSP00000415840.2:n.372+13G>A
ENST00000429746.1:c.303+13G>A	ENSP00000402586.1:n.303+13G>A
ENST00000433655.5:c.*138+13G>A	ENSP00000404902.1:n.*138+13G>A
ENST00000497544.1:n.601G>A
NM_001909.4:c.972+13G>A	NP_001900.1:n.972+13G>A
NM_001909.5:c.972+13G>A MANE Select	NP_001900.1:n.972+13G>A