Canonical Allele Identifier: CA471986109

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1757470T>G , CM000673.2:g.1757470T>G	GRCh38
NC_000011.9:g.1778700T>G , CM000673.1:g.1778700T>G	GRCh37
NC_000011.8:g.1735276T>G	NCBI36
NG_008655.1:g.11523A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001909.5:c.558A>C MANE Select	NP_001900.1:p.Pro186=
ENST00000236671.7:c.558A>C MANE Select	ENSP00000236671.2:p.Pro186=
NM_001909.4:c.558A>C	NP_001900.1:p.Pro186=
ENST00000236671.6:c.558A>C	ENSP00000236671.2:p.Pro186=
ENST00000367196.3:c.453A>C	ENSP00000356164.3:p.Pro151=
ENST00000367196.4:c.453A>C	ENSP00000356164.4:p.Pro151=
ENST00000427721.2:c.-43A>C	ENSP00000415840.2:n.-43A>C
ENST00000429746.2:c.453A>C	ENSP00000402586.2:p.Pro151=
ENST00000433655.5:c.558A>C	ENSP00000404902.1:p.Pro186=
ENST00000433655.6:c.558A>C	ENSP00000404902.1:p.Pro186=
ENST00000438213.5:c.513A>C	ENSP00000415036.1:p.Pro171=
ENST00000438213.6:c.558A>C	ENSP00000415036.2:p.Pro186=
ENST00000636397.1:c.558A>C	ENSP00000489910.1:p.Pro186=
ENST00000636571.1:c.537A>C	ENSP00000490770.1:p.Pro179=
ENST00000636615.1:c.558A>C	ENSP00000490014.1:p.Pro186=
ENST00000636843.1:c.552A>C	ENSP00000490897.1:p.Pro184=
ENST00000637158.1:n.156A>C
ENST00000637381.2:n.2986A>C
ENST00000637387.1:c.558A>C	ENSP00000490598.1:p.Pro186=
ENST00000637815.2:c.558A>C	ENSP00000490344.1:p.Pro186=
ENST00000637915.1:c.558A>C	ENSP00000490471.1:p.Pro186=
ENST00000677300.1:n.953A>C
ENST00000678991.1:c.*419A>C	ENSP00000503019.1:n.*419A>C