Canonical Allele Identifier: CA1947825157

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753651G= , CM000673.2:g.1753651G=	GRCh38
NC_000011.9:g.1774881G= , CM000673.1:g.1774881G=	GRCh37
NC_000011.8:g.1731457G=	NCBI36
NG_008655.1:g.15342C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1091C= MANE Select	ENSP00000236671.2:p.Thr364=
ENST00000367196.4:c.986C=	ENSP00000356164.4:p.Thr329=
ENST00000427721.3:c.516C=
ENST00000429746.2:c.986C=	ENSP00000402586.2:p.Thr329=
ENST00000433655.6:c.*257C=	ENSP00000404902.1:n.*257C=
ENST00000438213.6:c.1208C=	ENSP00000415036.2:p.Thr403=
ENST00000636397.1:c.1071+152C=	ENSP00000489910.1:n.1071+152C=
ENST00000636571.1:c.1070C=	ENSP00000490770.1:p.Thr357=
ENST00000636579.1:c.72+152C=	ENSP00000490489.1:n.72+152C=
ENST00000636615.1:c.1071+152C=	ENSP00000490014.1:n.1071+152C=
ENST00000636843.1:c.1085C=	ENSP00000490897.1:p.Thr362=
ENST00000637158.1:n.689C=
ENST00000637381.2:n.3519C=
ENST00000637387.1:c.1070C=	ENSP00000490598.1:p.Thr357=
ENST00000637815.2:c.1073C=	ENSP00000490344.1:p.Thr358=
ENST00000637915.1:c.1082C=	ENSP00000490471.1:p.Thr361=
ENST00000637937.1:n.399C=
ENST00000678991.1:c.*952C=	ENSP00000503019.1:n.*952C=
ENST00000236671.6:c.1091C=	ENSP00000236671.2:p.Thr364=
ENST00000427721.2:c.471+152C=	ENSP00000415840.2:n.471+152C=
ENST00000429746.1:c.422C=	ENSP00000402586.1:p.Thr141=
ENST00000433655.5:c.*257C=	ENSP00000404902.1:n.*257C=
NM_001909.4:c.1091C=	NP_001900.1:p.Thr364=
NM_001909.5:c.1091C= MANE Select	NP_001900.1:p.Thr364=