Canonical Allele Identifier: CA1947825070

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753482G= , CM000673.2:g.1753482G=	GRCh38
NC_000011.9:g.1774712G= , CM000673.1:g.1774712G=	GRCh37
NC_000011.8:g.1731288G=	NCBI36
NG_008655.1:g.15511C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*21C= MANE Select	ENSP00000236671.2:n.*21C=
ENST00000367196.4:c.*21C=	ENSP00000356164.4:n.*21C=
ENST00000427721.3:c.634+51C=
ENST00000429746.2:c.*21C=	ENSP00000402586.2:n.*21C=
ENST00000433655.6:c.*426C=	ENSP00000404902.1:n.*426C=
ENST00000438213.6:c.*21C=	ENSP00000415036.2:n.*21C=
ENST00000636397.1:c.1071+321C=	ENSP00000489910.1:n.1071+321C=
ENST00000636571.1:c.*21C=	ENSP00000490770.1:n.*21C=
ENST00000636579.1:c.72+321C=	ENSP00000490489.1:n.72+321C=
ENST00000636615.1:c.1071+321C=	ENSP00000490014.1:n.1071+321C=
ENST00000636843.1:c.*21C=	ENSP00000490897.1:n.*21C=
ENST00000637158.1:n.858C=
ENST00000637381.2:n.3688C=
ENST00000637387.1:c.*21C=	ENSP00000490598.1:n.*21C=
ENST00000637815.2:c.*21C=	ENSP00000490344.1:n.*21C=
ENST00000637915.1:c.*21C=	ENSP00000490471.1:n.*21C=
ENST00000637937.1:n.568C=
ENST00000678991.1:c.*1121C=	ENSP00000503019.1:n.*1121C=
ENST00000236671.6:c.*21C=	ENSP00000236671.2:n.*21C=
ENST00000427721.2:c.471+321C=	ENSP00000415840.2:n.471+321C=
ENST00000429746.1:c.591C=	ENSP00000402586.1:n.591C=
ENST00000433655.5:c.*426C=	ENSP00000404902.1:n.*426C=
NM_001909.4:c.*21C=	NP_001900.1:n.*21C=
NM_001909.5:c.*21C= MANE Select	NP_001900.1:n.*21C=