Canonical Allele Identifier: CA1947825022

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753411T= , CM000673.2:g.1753411T=	GRCh38
NC_000011.9:g.1774641T= , CM000673.1:g.1774641T=	GRCh37
NC_000011.8:g.1731217T=	NCBI36
NG_008655.1:g.15582A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*92A= MANE Select	ENSP00000236671.2:n.*92A=
ENST00000367196.4:c.*92A=	ENSP00000356164.4:n.*92A=
ENST00000427721.3:c.634+122A=
ENST00000429746.2:c.*92A=	ENSP00000402586.2:n.*92A=
ENST00000433655.6:c.*497A=	ENSP00000404902.1:n.*497A=
ENST00000438213.6:c.*92A=	ENSP00000415036.2:n.*92A=
ENST00000636397.1:c.1071+392A=	ENSP00000489910.1:n.1071+392A=
ENST00000636571.1:c.*92A=	ENSP00000490770.1:n.*92A=
ENST00000636579.1:c.72+392A=	ENSP00000490489.1:n.72+392A=
ENST00000636615.1:c.1071+392A=	ENSP00000490014.1:n.1071+392A=
ENST00000636843.1:c.*92A=	ENSP00000490897.1:n.*92A=
ENST00000637158.1:n.929A=
ENST00000637381.2:n.3759A=
ENST00000637387.1:c.*92A=	ENSP00000490598.1:n.*92A=
ENST00000637815.2:c.*92A=	ENSP00000490344.1:n.*92A=
ENST00000637915.1:c.*92A=	ENSP00000490471.1:n.*92A=
ENST00000637937.1:n.639A=
ENST00000678991.1:c.*1192A=	ENSP00000503019.1:n.*1192A=
ENST00000236671.6:c.*92A=	ENSP00000236671.2:n.*92A=
ENST00000427721.2:c.471+392A=	ENSP00000415840.2:n.471+392A=
ENST00000429746.1:c.662A=	ENSP00000402586.1:n.662A=
ENST00000433655.5:c.*497A=	ENSP00000404902.1:n.*497A=
NM_001909.4:c.*92A=	NP_001900.1:n.*92A=
NM_001909.5:c.*92A= MANE Select	NP_001900.1:n.*92A=