Canonical Allele Identifier: CA1947825384

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754020C= , CM000673.2:g.1754020C=	GRCh38
NC_000011.9:g.1775250C= , CM000673.1:g.1775250C=	GRCh37
NC_000011.8:g.1731826C=	NCBI36
NG_008655.1:g.14973G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.946G= MANE Select	ENSP00000236671.2:p.Gly316=
ENST00000367196.4:c.841G=	ENSP00000356164.4:p.Gly281=
ENST00000427721.3:c.371G=
ENST00000429746.2:c.841G=	ENSP00000402586.2:p.Gly281=
ENST00000433655.6:c.*112G=	ENSP00000404902.1:n.*112G=
ENST00000438213.6:c.1063G=	ENSP00000415036.2:p.Gly355=
ENST00000497544.3:n.562G=
ENST00000636397.1:c.946G=	ENSP00000489910.1:p.Gly316=
ENST00000636571.1:c.925G=	ENSP00000490770.1:p.Gly309=
ENST00000636615.1:c.946G=	ENSP00000490014.1:p.Gly316=
ENST00000636843.1:c.940G=	ENSP00000490897.1:p.Gly314=
ENST00000637158.1:n.544G=
ENST00000637381.2:n.3374G=
ENST00000637387.1:c.946G=	ENSP00000490598.1:p.Gly316=
ENST00000637815.2:c.928G=	ENSP00000490344.1:p.Gly310=
ENST00000637915.1:c.946G=	ENSP00000490471.1:p.Gly316=
ENST00000637937.1:n.254G=
ENST00000678991.1:c.*807G=	ENSP00000503019.1:n.*807G=
ENST00000236671.6:c.946G=	ENSP00000236671.2:p.Gly316=
ENST00000427721.2:c.346G=	ENSP00000415840.2:p.Gly116=
ENST00000429746.1:c.277G=	ENSP00000402586.1:p.Gly93=
ENST00000433655.5:c.*112G=	ENSP00000404902.1:n.*112G=
ENST00000497544.1:n.562G=
NM_001909.4:c.946G=	NP_001900.1:p.Gly316=
NM_001909.5:c.946G= MANE Select	NP_001900.1:p.Gly316=