Canonical Allele Identifier: CA2739276111

Gene: CTSD

Linked Data

• ClinVar Variation Id: 2847451
• ClinVar RCV Id: RCV003648473

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753979G>T , CM000673.2:g.1753979G>T	GRCh38
NC_000011.9:g.1775209G>T , CM000673.1:g.1775209G>T	GRCh37
NC_000011.8:g.1731785G>T	NCBI36
NG_008655.1:g.15014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.972+15C>A MANE Select	ENSP00000236671.2:n.972+15C>A
ENST00000367196.4:c.867+15C>A	ENSP00000356164.4:n.867+15C>A
ENST00000427721.3:c.397+15C>A
ENST00000429746.2:c.867+15C>A	ENSP00000402586.2:n.867+15C>A
ENST00000433655.6:c.*138+15C>A	ENSP00000404902.1:n.*138+15C>A
ENST00000438213.6:c.1089+15C>A	ENSP00000415036.2:n.1089+15C>A
ENST00000497544.3:n.603C>A
ENST00000636397.1:c.972+15C>A	ENSP00000489910.1:n.972+15C>A
ENST00000636571.1:c.951+15C>A	ENSP00000490770.1:n.951+15C>A
ENST00000636615.1:c.972+15C>A	ENSP00000490014.1:n.972+15C>A
ENST00000636843.1:c.966+15C>A	ENSP00000490897.1:n.966+15C>A
ENST00000637158.1:n.570+15C>A
ENST00000637381.2:n.3400+15C>A
ENST00000637387.1:c.972+15C>A	ENSP00000490598.1:n.972+15C>A
ENST00000637815.2:c.954+15C>A	ENSP00000490344.1:n.954+15C>A
ENST00000637915.1:c.972+15C>A	ENSP00000490471.1:n.972+15C>A
ENST00000637937.1:n.280+15C>A
ENST00000678991.1:c.*833+15C>A	ENSP00000503019.1:n.*833+15C>A
ENST00000236671.6:c.972+15C>A	ENSP00000236671.2:n.972+15C>A
ENST00000427721.2:c.372+15C>A	ENSP00000415840.2:n.372+15C>A
ENST00000429746.1:c.303+15C>A	ENSP00000402586.1:n.303+15C>A
ENST00000433655.5:c.*138+15C>A	ENSP00000404902.1:n.*138+15C>A
ENST00000497544.1:n.603C>A
NM_001909.4:c.972+15C>A	NP_001900.1:n.972+15C>A
NM_001909.5:c.972+15C>A MANE Select	NP_001900.1:n.972+15C>A