Canonical Allele Identifier: CA1947828423

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1758975_1758976delinsAG , CM000673.2:g.1758975_1758976delinsAG	GRCh38
NC_000011.9:g.1780205_1780206delinsAG , CM000673.1:g.1780205_1780206delinsAG	GRCh37
NC_000011.8:g.1736781_1736782delinsAG	NCBI36
NG_008655.1:g.10017_10018delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.464_465delinsCT MANE Select	ENSP00000236671.2:p.Thr155=
ENST00000367196.4:c.359_360delinsCT	ENSP00000356164.4:p.Thr120=
ENST00000429746.2:c.359_360delinsCT	ENSP00000402586.2:p.Thr120=
ENST00000433655.6:c.464_465delinsCT	ENSP00000404902.1:p.Thr155=
ENST00000438213.6:c.464_465delinsCT	ENSP00000415036.2:p.Thr155=
ENST00000636397.1:c.464_465delinsCT	ENSP00000489910.1:p.Thr155=
ENST00000636571.1:c.443_444delinsCT	ENSP00000490770.1:p.Thr148=
ENST00000636615.1:c.464_465delinsCT	ENSP00000490014.1:p.Thr155=
ENST00000636843.1:c.458_459delinsCT	ENSP00000490897.1:p.Thr153=
ENST00000637381.2:n.2892_2893delinsCT
ENST00000637387.1:c.464_465delinsCT	ENSP00000490598.1:p.Thr155=
ENST00000637815.2:c.464_465delinsCT	ENSP00000490344.1:p.Thr155=
ENST00000637915.1:c.464_465delinsCT	ENSP00000490471.1:p.Thr155=
ENST00000677300.1:n.859_860delinsCT
ENST00000678991.1:c.*325_*326delinsCT	ENSP00000503019.1:n.*325_*326delinsCT
ENST00000236671.6:c.464_465delinsCT	ENSP00000236671.2:p.Thr155=
ENST00000367196.3:c.359_360delinsCT	ENSP00000356164.3:p.Thr120=
ENST00000427721.2:c.-137_-136delinsCT	ENSP00000415840.2:n.-137_-136delinsCT
ENST00000433655.5:c.464_465delinsCT	ENSP00000404902.1:p.Thr155=
ENST00000438213.5:c.419_420delinsCT	ENSP00000415036.1:p.Thr140=
NM_001909.4:c.464_465delinsCT	NP_001900.1:p.Thr155=
NM_001909.5:c.464_465delinsCT MANE Select	NP_001900.1:p.Thr155=