Canonical Allele Identifier: CA2790175887

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759642G>C , CM000673.2:g.1759642G>C	GRCh38
NC_000011.9:g.1780872G>C , CM000673.1:g.1780872G>C	GRCh37
NC_000011.8:g.1737448G>C	NCBI36
NG_008655.1:g.9351C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.229-3C>G MANE Select	ENSP00000236671.2:n.229-3C>G
ENST00000367196.4:c.124-3C>G	ENSP00000356164.4:n.124-3C>G
ENST00000429746.2:c.124-3C>G	ENSP00000402586.2:n.124-3C>G
ENST00000433655.6:c.229-3C>G	ENSP00000404902.1:n.229-3C>G
ENST00000438213.6:c.229-3C>G	ENSP00000415036.2:n.229-3C>G
ENST00000636397.1:c.229-3C>G	ENSP00000489910.1:n.229-3C>G
ENST00000636571.1:c.208-3C>G	ENSP00000490770.1:n.208-3C>G
ENST00000636615.1:c.229-3C>G	ENSP00000490014.1:n.229-3C>G
ENST00000636843.1:c.229-9C>G	ENSP00000490897.1:n.229-9C>G
ENST00000637381.2:n.2657-3C>G
ENST00000637387.1:c.229-3C>G	ENSP00000490598.1:n.229-3C>G
ENST00000637815.2:c.229-3C>G	ENSP00000490344.1:n.229-3C>G
ENST00000637915.1:c.229-3C>G	ENSP00000490471.1:n.229-3C>G
ENST00000677300.1:n.624-3C>G
ENST00000678991.1:c.*90-3C>G	ENSP00000503019.1:n.*90-3C>G
ENST00000236671.6:c.229-3C>G	ENSP00000236671.2:n.229-3C>G
ENST00000367196.3:c.124-3C>G	ENSP00000356164.3:n.124-3C>G
ENST00000433655.5:c.229-3C>G	ENSP00000404902.1:n.229-3C>G
ENST00000438213.5:c.184-3C>G	ENSP00000415036.1:n.184-3C>G
NM_001909.4:c.229-3C>G	NP_001900.1:n.229-3C>G
NM_001909.5:c.229-3C>G MANE Select	NP_001900.1:n.229-3C>G