Canonical Allele Identifier: CA1947825161

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753661C= , CM000673.2:g.1753661C=	GRCh38
NC_000011.9:g.1774891C= , CM000673.1:g.1774891C=	GRCh37
NC_000011.8:g.1731467C=	NCBI36
NG_008655.1:g.15332G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1081G= MANE Select	ENSP00000236671.2:p.Ala361=
ENST00000367196.4:c.976G=	ENSP00000356164.4:p.Ala326=
ENST00000427721.3:c.506G=
ENST00000429746.2:c.976G=	ENSP00000402586.2:p.Ala326=
ENST00000433655.6:c.*247G=	ENSP00000404902.1:n.*247G=
ENST00000438213.6:c.1198G=	ENSP00000415036.2:p.Ala400=
ENST00000497544.3:n.789G=
ENST00000636397.1:c.1071+142G=	ENSP00000489910.1:n.1071+142G=
ENST00000636571.1:c.1060G=	ENSP00000490770.1:p.Ala354=
ENST00000636579.1:c.72+142G=	ENSP00000490489.1:n.72+142G=
ENST00000636615.1:c.1071+142G=	ENSP00000490014.1:n.1071+142G=
ENST00000636843.1:c.1075G=	ENSP00000490897.1:p.Ala359=
ENST00000637158.1:n.679G=
ENST00000637381.2:n.3509G=
ENST00000637387.1:c.1060G=	ENSP00000490598.1:p.Ala354=
ENST00000637815.2:c.1063G=	ENSP00000490344.1:p.Ala355=
ENST00000637915.1:c.1072G=	ENSP00000490471.1:p.Ala358=
ENST00000637937.1:n.389G=
ENST00000678991.1:c.*942G=	ENSP00000503019.1:n.*942G=
ENST00000236671.6:c.1081G=	ENSP00000236671.2:p.Ala361=
ENST00000427721.2:c.471+142G=	ENSP00000415840.2:n.471+142G=
ENST00000429746.1:c.412G=	ENSP00000402586.1:p.Ala138=
ENST00000433655.5:c.*247G=	ENSP00000404902.1:n.*247G=
NM_001909.4:c.1081G=	NP_001900.1:p.Ala361=
NM_001909.5:c.1081G= MANE Select	NP_001900.1:p.Ala361=