Canonical Allele Identifier: CA1947825299

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753884C= , CM000673.2:g.1753884C=	GRCh38
NC_000011.9:g.1775114C= , CM000673.1:g.1775114C=	GRCh37
NC_000011.8:g.1731690C=	NCBI36
NG_008655.1:g.15109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.990G= MANE Select	ENSP00000236671.2:p.Glu330=
ENST00000367196.4:c.885G=	ENSP00000356164.4:p.Glu295=
ENST00000427721.3:c.415G=
ENST00000429746.2:c.885G=	ENSP00000402586.2:p.Glu295=
ENST00000433655.6:c.*156G=	ENSP00000404902.1:n.*156G=
ENST00000438213.6:c.1107G=	ENSP00000415036.2:p.Glu369=
ENST00000497544.3:n.698G=
ENST00000636397.1:c.990G=	ENSP00000489910.1:p.Glu330=
ENST00000636571.1:c.969G=	ENSP00000490770.1:p.Glu323=
ENST00000636615.1:c.990G=	ENSP00000490014.1:p.Glu330=
ENST00000636843.1:c.984G=	ENSP00000490897.1:p.Glu328=
ENST00000637158.1:n.588G=
ENST00000637381.2:n.3418G=
ENST00000637387.1:c.973-4G=	ENSP00000490598.1:n.973-4G=
ENST00000637815.2:c.972G=	ENSP00000490344.1:p.Glu324=
ENST00000637915.1:c.990G=	ENSP00000490471.1:p.Glu330=
ENST00000637937.1:n.298G=
ENST00000678991.1:c.*851G=	ENSP00000503019.1:n.*851G=
ENST00000236671.6:c.990G=	ENSP00000236671.2:p.Glu330=
ENST00000427721.2:c.390G=	ENSP00000415840.2:p.Glu130=
ENST00000429746.1:c.321G=	ENSP00000402586.1:p.Glu107=
ENST00000433655.5:c.*156G=	ENSP00000404902.1:n.*156G=
ENST00000497544.1:n.698G=
NM_001909.4:c.990G=	NP_001900.1:p.Glu330=
NM_001909.5:c.990G= MANE Select	NP_001900.1:p.Glu330=