Canonical Allele Identifier: CA1947825093

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753519T= , CM000673.2:g.1753519T=	GRCh38
NC_000011.9:g.1774749T= , CM000673.1:g.1774749T=	GRCh37
NC_000011.8:g.1731325T=	NCBI36
NG_008655.1:g.15474A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1223A= MANE Select	ENSP00000236671.2:p.Glu408=
ENST00000367196.4:c.1118A=	ENSP00000356164.4:p.Glu373=
ENST00000427721.3:c.634+14A=
ENST00000429746.2:c.1118A=	ENSP00000402586.2:p.Glu373=
ENST00000433655.6:c.*389A=	ENSP00000404902.1:n.*389A=
ENST00000438213.6:c.1340A=	ENSP00000415036.2:p.Glu447=
ENST00000636397.1:c.1071+284A=	ENSP00000489910.1:n.1071+284A=
ENST00000636571.1:c.1202A=	ENSP00000490770.1:p.Glu401=
ENST00000636579.1:c.72+284A=	ENSP00000490489.1:n.72+284A=
ENST00000636615.1:c.1071+284A=	ENSP00000490014.1:n.1071+284A=
ENST00000636843.1:c.1217A=	ENSP00000490897.1:p.Glu406=
ENST00000637158.1:n.821A=
ENST00000637381.2:n.3651A=
ENST00000637387.1:c.1202A=	ENSP00000490598.1:p.Glu401=
ENST00000637815.2:c.1205A=	ENSP00000490344.1:p.Glu402=
ENST00000637915.1:c.1214A=	ENSP00000490471.1:p.Glu405=
ENST00000637937.1:n.531A=
ENST00000678991.1:c.*1084A=	ENSP00000503019.1:n.*1084A=
ENST00000236671.6:c.1223A=	ENSP00000236671.2:p.Glu408=
ENST00000427721.2:c.471+284A=	ENSP00000415840.2:n.471+284A=
ENST00000429746.1:c.554A=	ENSP00000402586.1:p.Glu185=
ENST00000433655.5:c.*389A=	ENSP00000404902.1:n.*389A=
NM_001909.4:c.1223A=	NP_001900.1:p.Glu408=
NM_001909.5:c.1223A= MANE Select	NP_001900.1:p.Glu408=