Canonical Allele Identifier: CA1947825119

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753571C= , CM000673.2:g.1753571C=	GRCh38
NC_000011.9:g.1774801C= , CM000673.1:g.1774801C=	GRCh37
NC_000011.8:g.1731377C=	NCBI36
NG_008655.1:g.15422G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1171G= MANE Select	ENSP00000236671.2:p.Gly391=
ENST00000367196.4:c.1066G=	ENSP00000356164.4:p.Gly356=
ENST00000427721.3:c.596G=
ENST00000429746.2:c.1066G=	ENSP00000402586.2:p.Gly356=
ENST00000433655.6:c.*337G=	ENSP00000404902.1:n.*337G=
ENST00000438213.6:c.1288G=	ENSP00000415036.2:p.Gly430=
ENST00000636397.1:c.1071+232G=	ENSP00000489910.1:n.1071+232G=
ENST00000636571.1:c.1150G=	ENSP00000490770.1:p.Gly384=
ENST00000636579.1:c.72+232G=	ENSP00000490489.1:n.72+232G=
ENST00000636615.1:c.1071+232G=	ENSP00000490014.1:n.1071+232G=
ENST00000636843.1:c.1165G=	ENSP00000490897.1:p.Gly389=
ENST00000637158.1:n.769G=
ENST00000637381.2:n.3599G=
ENST00000637387.1:c.1150G=	ENSP00000490598.1:p.Gly384=
ENST00000637815.2:c.1153G=	ENSP00000490344.1:p.Gly385=
ENST00000637915.1:c.1162G=	ENSP00000490471.1:p.Gly388=
ENST00000637937.1:n.479G=
ENST00000678991.1:c.*1032G=	ENSP00000503019.1:n.*1032G=
ENST00000236671.6:c.1171G=	ENSP00000236671.2:p.Gly391=
ENST00000427721.2:c.471+232G=	ENSP00000415840.2:n.471+232G=
ENST00000429746.1:c.502G=	ENSP00000402586.1:p.Gly168=
ENST00000433655.5:c.*337G=	ENSP00000404902.1:n.*337G=
NM_001909.4:c.1171G=	NP_001900.1:p.Gly391=
NM_001909.5:c.1171G= MANE Select	NP_001900.1:p.Gly391=