Canonical Allele Identifier: CA1947825107

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753546C= , CM000673.2:g.1753546C=	GRCh38
NC_000011.9:g.1774776C= , CM000673.1:g.1774776C=	GRCh37
NC_000011.8:g.1731352C=	NCBI36
NG_008655.1:g.15447G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1196G= MANE Select	ENSP00000236671.2:p.Arg399=
ENST00000367196.4:c.1091G=	ENSP00000356164.4:p.Arg364=
ENST00000427721.3:c.621G=
ENST00000429746.2:c.1091G=	ENSP00000402586.2:p.Arg364=
ENST00000433655.6:c.*362G=	ENSP00000404902.1:n.*362G=
ENST00000438213.6:c.1313G=	ENSP00000415036.2:p.Arg438=
ENST00000636397.1:c.1071+257G=	ENSP00000489910.1:n.1071+257G=
ENST00000636571.1:c.1175G=	ENSP00000490770.1:p.Arg392=
ENST00000636579.1:c.72+257G=	ENSP00000490489.1:n.72+257G=
ENST00000636615.1:c.1071+257G=	ENSP00000490014.1:n.1071+257G=
ENST00000636843.1:c.1190G=	ENSP00000490897.1:p.Arg397=
ENST00000637158.1:n.794G=
ENST00000637381.2:n.3624G=
ENST00000637387.1:c.1175G=	ENSP00000490598.1:p.Arg392=
ENST00000637815.2:c.1178G=	ENSP00000490344.1:p.Arg393=
ENST00000637915.1:c.1187G=	ENSP00000490471.1:p.Arg396=
ENST00000637937.1:n.504G=
ENST00000678991.1:c.*1057G=	ENSP00000503019.1:n.*1057G=
ENST00000236671.6:c.1196G=	ENSP00000236671.2:p.Arg399=
ENST00000427721.2:c.471+257G=	ENSP00000415840.2:n.471+257G=
ENST00000429746.1:c.527G=	ENSP00000402586.1:p.Arg176=
ENST00000433655.5:c.*362G=	ENSP00000404902.1:n.*362G=
NM_001909.4:c.1196G=	NP_001900.1:p.Arg399=
NM_001909.5:c.1196G= MANE Select	NP_001900.1:p.Arg399=