Canonical Allele Identifier: CA1947825168

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753675G= , CM000673.2:g.1753675G=	GRCh38
NC_000011.9:g.1774905G= , CM000673.1:g.1774905G=	GRCh37
NC_000011.8:g.1731481G=	NCBI36
NG_008655.1:g.15318C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1072-5C= MANE Select	ENSP00000236671.2:n.1072-5C=
ENST00000367196.4:c.967-5C=	ENSP00000356164.4:n.967-5C=
ENST00000427721.3:c.497-5C=
ENST00000429746.2:c.967-5C=	ENSP00000402586.2:n.967-5C=
ENST00000433655.6:c.*238-5C=	ENSP00000404902.1:n.*238-5C=
ENST00000438213.6:c.1189-5C=	ENSP00000415036.2:n.1189-5C=
ENST00000497544.3:n.780-5C=
ENST00000636397.1:c.1071+128C=	ENSP00000489910.1:n.1071+128C=
ENST00000636571.1:c.1051-5C=	ENSP00000490770.1:n.1051-5C=
ENST00000636579.1:c.72+128C=	ENSP00000490489.1:n.72+128C=
ENST00000636615.1:c.1071+128C=	ENSP00000490014.1:n.1071+128C=
ENST00000636843.1:c.1066-5C=	ENSP00000490897.1:n.1066-5C=
ENST00000637158.1:n.670-5C=
ENST00000637381.2:n.3500-5C=
ENST00000637387.1:c.1051-5C=	ENSP00000490598.1:n.1051-5C=
ENST00000637815.2:c.1054-5C=	ENSP00000490344.1:n.1054-5C=
ENST00000637915.1:c.1072-14C=	ENSP00000490471.1:n.1072-14C=
ENST00000637937.1:n.380-5C=
ENST00000678991.1:c.*933-5C=	ENSP00000503019.1:n.*933-5C=
ENST00000236671.6:c.1072-5C=	ENSP00000236671.2:n.1072-5C=
ENST00000427721.2:c.471+128C=	ENSP00000415840.2:n.471+128C=
ENST00000429746.1:c.403-5C=	ENSP00000402586.1:n.403-5C=
ENST00000433655.5:c.*238-5C=	ENSP00000404902.1:n.*238-5C=
NM_001909.4:c.1072-5C=	NP_001900.1:n.1072-5C=
NM_001909.5:c.1072-5C= MANE Select	NP_001900.1:n.1072-5C=