Canonical Allele Identifier: CA1947825162

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753664G= , CM000673.2:g.1753664G=	GRCh38
NC_000011.9:g.1774894G= , CM000673.1:g.1774894G=	GRCh37
NC_000011.8:g.1731470G=	NCBI36
NG_008655.1:g.15329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1078C= MANE Select	ENSP00000236671.2:p.Gln360=
ENST00000367196.4:c.973C=	ENSP00000356164.4:p.Gln325=
ENST00000427721.3:c.503C=
ENST00000429746.2:c.973C=	ENSP00000402586.2:p.Gln325=
ENST00000433655.6:c.*244C=	ENSP00000404902.1:n.*244C=
ENST00000438213.6:c.1195C=	ENSP00000415036.2:p.Gln399=
ENST00000497544.3:n.786C=
ENST00000636397.1:c.1071+139C=	ENSP00000489910.1:n.1071+139C=
ENST00000636571.1:c.1057C=	ENSP00000490770.1:p.Gln353=
ENST00000636579.1:c.72+139C=	ENSP00000490489.1:n.72+139C=
ENST00000636615.1:c.1071+139C=	ENSP00000490014.1:n.1071+139C=
ENST00000636843.1:c.1072C=	ENSP00000490897.1:p.Gln358=
ENST00000637158.1:n.676C=
ENST00000637381.2:n.3506C=
ENST00000637387.1:c.1057C=	ENSP00000490598.1:p.Gln353=
ENST00000637815.2:c.1060C=	ENSP00000490344.1:p.Gln354=
ENST00000637915.1:c.1072-3C=	ENSP00000490471.1:n.1072-3C=
ENST00000637937.1:n.386C=
ENST00000678991.1:c.*939C=	ENSP00000503019.1:n.*939C=
ENST00000236671.6:c.1078C=	ENSP00000236671.2:p.Gln360=
ENST00000427721.2:c.471+139C=	ENSP00000415840.2:n.471+139C=
ENST00000429746.1:c.409C=	ENSP00000402586.1:p.Gln137=
ENST00000433655.5:c.*244C=	ENSP00000404902.1:n.*244C=
NM_001909.4:c.1078C=	NP_001900.1:p.Gln360=
NM_001909.5:c.1078C= MANE Select	NP_001900.1:p.Gln360=