Canonical Allele Identifier: CA1947825303

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753891G= , CM000673.2:g.1753891G=	GRCh38
NC_000011.9:g.1775121G= , CM000673.1:g.1775121G=	GRCh37
NC_000011.8:g.1731697G=	NCBI36
NG_008655.1:g.15102C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.983C= MANE Select	ENSP00000236671.2:p.Pro328=
ENST00000367196.4:c.878C=	ENSP00000356164.4:p.Pro293=
ENST00000427721.3:c.408C=
ENST00000429746.2:c.878C=	ENSP00000402586.2:p.Pro293=
ENST00000433655.6:c.*149C=	ENSP00000404902.1:n.*149C=
ENST00000438213.6:c.1100C=	ENSP00000415036.2:p.Pro367=
ENST00000497544.3:n.691C=
ENST00000636397.1:c.983C=	ENSP00000489910.1:p.Pro328=
ENST00000636571.1:c.962C=	ENSP00000490770.1:p.Pro321=
ENST00000636615.1:c.983C=	ENSP00000490014.1:p.Pro328=
ENST00000636843.1:c.977C=	ENSP00000490897.1:p.Pro326=
ENST00000637158.1:n.581C=
ENST00000637381.2:n.3411C=
ENST00000637387.1:c.973-11C=	ENSP00000490598.1:n.973-11C=
ENST00000637815.2:c.965C=	ENSP00000490344.1:p.Pro322=
ENST00000637915.1:c.983C=	ENSP00000490471.1:p.Pro328=
ENST00000637937.1:n.291C=
ENST00000678991.1:c.*844C=	ENSP00000503019.1:n.*844C=
ENST00000236671.6:c.983C=	ENSP00000236671.2:p.Pro328=
ENST00000427721.2:c.383C=	ENSP00000415840.2:p.Pro128=
ENST00000429746.1:c.314C=	ENSP00000402586.1:p.Pro105=
ENST00000433655.5:c.*149C=	ENSP00000404902.1:n.*149C=
ENST00000497544.1:n.691C=
NM_001909.4:c.983C=	NP_001900.1:p.Pro328=
NM_001909.5:c.983C= MANE Select	NP_001900.1:p.Pro328=