Canonical Allele Identifier: CA1947825094

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753520C= , CM000673.2:g.1753520C=	GRCh38
NC_000011.9:g.1774750C= , CM000673.1:g.1774750C=	GRCh37
NC_000011.8:g.1731326C=	NCBI36
NG_008655.1:g.15473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1222G= MANE Select	ENSP00000236671.2:p.Glu408=
ENST00000367196.4:c.1117G=	ENSP00000356164.4:p.Glu373=
ENST00000427721.3:c.634+13G=
ENST00000429746.2:c.1117G=	ENSP00000402586.2:p.Glu373=
ENST00000433655.6:c.*388G=	ENSP00000404902.1:n.*388G=
ENST00000438213.6:c.1339G=	ENSP00000415036.2:p.Glu447=
ENST00000636397.1:c.1071+283G=	ENSP00000489910.1:n.1071+283G=
ENST00000636571.1:c.1201G=	ENSP00000490770.1:p.Glu401=
ENST00000636579.1:c.72+283G=	ENSP00000490489.1:n.72+283G=
ENST00000636615.1:c.1071+283G=	ENSP00000490014.1:n.1071+283G=
ENST00000636843.1:c.1216G=	ENSP00000490897.1:p.Glu406=
ENST00000637158.1:n.820G=
ENST00000637381.2:n.3650G=
ENST00000637387.1:c.1201G=	ENSP00000490598.1:p.Glu401=
ENST00000637815.2:c.1204G=	ENSP00000490344.1:p.Glu402=
ENST00000637915.1:c.1213G=	ENSP00000490471.1:p.Glu405=
ENST00000637937.1:n.530G=
ENST00000678991.1:c.*1083G=	ENSP00000503019.1:n.*1083G=
ENST00000236671.6:c.1222G=	ENSP00000236671.2:p.Glu408=
ENST00000427721.2:c.471+283G=	ENSP00000415840.2:n.471+283G=
ENST00000429746.1:c.553G=	ENSP00000402586.1:p.Glu185=
ENST00000433655.5:c.*388G=	ENSP00000404902.1:n.*388G=
NM_001909.4:c.1222G=	NP_001900.1:p.Glu408=
NM_001909.5:c.1222G= MANE Select	NP_001900.1:p.Glu408=