Canonical Allele Identifier: CA5814250

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759658C>T , CM000673.2:g.1759658C>T	GRCh38
NC_000011.9:g.1780888C>T , CM000673.1:g.1780888C>T	GRCh37
NC_000011.8:g.1737464C>T	NCBI36
NG_008655.1:g.9335G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001909.5:c.229-19G>A MANE Select	NP_001900.1:n.229-19G>A
ENST00000236671.7:c.229-19G>A MANE Select	ENSP00000236671.2:n.229-19G>A
NM_001909.4:c.229-19G>A	NP_001900.1:n.229-19G>A
ENST00000236671.6:c.229-19G>A	ENSP00000236671.2:n.229-19G>A
ENST00000367196.3:c.124-19G>A	ENSP00000356164.3:n.124-19G>A
ENST00000367196.4:c.124-19G>A	ENSP00000356164.4:n.124-19G>A
ENST00000429746.2:c.124-19G>A	ENSP00000402586.2:n.124-19G>A
ENST00000433655.5:c.229-19G>A	ENSP00000404902.1:n.229-19G>A
ENST00000433655.6:c.229-19G>A	ENSP00000404902.1:n.229-19G>A
ENST00000438213.5:c.184-19G>A	ENSP00000415036.1:n.184-19G>A
ENST00000438213.6:c.229-19G>A	ENSP00000415036.2:n.229-19G>A
ENST00000636397.1:c.229-19G>A	ENSP00000489910.1:n.229-19G>A
ENST00000636571.1:c.208-19G>A	ENSP00000490770.1:n.208-19G>A
ENST00000636615.1:c.229-19G>A	ENSP00000490014.1:n.229-19G>A
ENST00000636843.1:c.229-25G>A	ENSP00000490897.1:n.229-25G>A
ENST00000637381.2:n.2657-19G>A
ENST00000637387.1:c.229-19G>A	ENSP00000490598.1:n.229-19G>A
ENST00000637815.2:c.229-19G>A	ENSP00000490344.1:n.229-19G>A
ENST00000637915.1:c.229-19G>A	ENSP00000490471.1:n.229-19G>A
ENST00000677300.1:n.624-19G>A
ENST00000678991.1:c.*90-19G>A	ENSP00000503019.1:n.*90-19G>A