Canonical Allele Identifier: CA1947825149

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753626G= , CM000673.2:g.1753626G=	GRCh38
NC_000011.9:g.1774856G= , CM000673.1:g.1774856G=	GRCh37
NC_000011.8:g.1731432G=	NCBI36
NG_008655.1:g.15367C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1116C= MANE Select	ENSP00000236671.2:p.Gly372=
ENST00000367196.4:c.1011C=	ENSP00000356164.4:p.Gly337=
ENST00000427721.3:c.541C=
ENST00000429746.2:c.1011C=	ENSP00000402586.2:p.Gly337=
ENST00000433655.6:c.*282C=	ENSP00000404902.1:n.*282C=
ENST00000438213.6:c.1233C=	ENSP00000415036.2:p.Gly411=
ENST00000636397.1:c.1071+177C=	ENSP00000489910.1:n.1071+177C=
ENST00000636571.1:c.1095C=	ENSP00000490770.1:p.Gly365=
ENST00000636579.1:c.72+177C=	ENSP00000490489.1:n.72+177C=
ENST00000636615.1:c.1071+177C=	ENSP00000490014.1:n.1071+177C=
ENST00000636843.1:c.1110C=	ENSP00000490897.1:p.Gly370=
ENST00000637158.1:n.714C=
ENST00000637381.2:n.3544C=
ENST00000637387.1:c.1095C=	ENSP00000490598.1:p.Gly365=
ENST00000637815.2:c.1098C=	ENSP00000490344.1:p.Gly366=
ENST00000637915.1:c.1107C=	ENSP00000490471.1:p.Gly369=
ENST00000637937.1:n.424C=
ENST00000678991.1:c.*977C=	ENSP00000503019.1:n.*977C=
ENST00000236671.6:c.1116C=	ENSP00000236671.2:p.Gly372=
ENST00000427721.2:c.471+177C=	ENSP00000415840.2:n.471+177C=
ENST00000429746.1:c.447C=	ENSP00000402586.1:p.Gly149=
ENST00000433655.5:c.*282C=	ENSP00000404902.1:n.*282C=
NM_001909.4:c.1116C=	NP_001900.1:p.Gly372=
NM_001909.5:c.1116C= MANE Select	NP_001900.1:p.Gly372=