Canonical Allele Identifier: CA1947825378

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754010G= , CM000673.2:g.1754010G=	GRCh38
NC_000011.9:g.1775240G= , CM000673.1:g.1775240G=	GRCh37
NC_000011.8:g.1731816G=	NCBI36
NG_008655.1:g.14983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.956C= MANE Select	ENSP00000236671.2:p.Pro319=
ENST00000367196.4:c.851C=	ENSP00000356164.4:p.Pro284=
ENST00000427721.3:c.381C=
ENST00000429746.2:c.851C=	ENSP00000402586.2:p.Pro284=
ENST00000433655.6:c.*122C=	ENSP00000404902.1:n.*122C=
ENST00000438213.6:c.1073C=	ENSP00000415036.2:p.Pro358=
ENST00000497544.3:n.572C=
ENST00000636397.1:c.956C=	ENSP00000489910.1:p.Pro319=
ENST00000636571.1:c.935C=	ENSP00000490770.1:p.Pro312=
ENST00000636615.1:c.956C=	ENSP00000490014.1:p.Pro319=
ENST00000636843.1:c.950C=	ENSP00000490897.1:p.Pro317=
ENST00000637158.1:n.554C=
ENST00000637381.2:n.3384C=
ENST00000637387.1:c.956C=	ENSP00000490598.1:p.Pro319=
ENST00000637815.2:c.938C=	ENSP00000490344.1:p.Pro313=
ENST00000637915.1:c.956C=	ENSP00000490471.1:p.Pro319=
ENST00000637937.1:n.264C=
ENST00000678991.1:c.*817C=	ENSP00000503019.1:n.*817C=
ENST00000236671.6:c.956C=	ENSP00000236671.2:p.Pro319=
ENST00000427721.2:c.356C=	ENSP00000415840.2:p.Pro119=
ENST00000429746.1:c.287C=	ENSP00000402586.1:p.Pro96=
ENST00000433655.5:c.*122C=	ENSP00000404902.1:n.*122C=
ENST00000497544.1:n.572C=
NM_001909.4:c.956C=	NP_001900.1:p.Pro319=
NM_001909.5:c.956C= MANE Select	NP_001900.1:p.Pro319=