Canonical Allele Identifier: CA1947825064

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753469C= , CM000673.2:g.1753469C=	GRCh38
NC_000011.9:g.1774699C= , CM000673.1:g.1774699C=	GRCh37
NC_000011.8:g.1731275C=	NCBI36
NG_008655.1:g.15524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*34G= MANE Select	ENSP00000236671.2:n.*34G=
ENST00000367196.4:c.*34G=	ENSP00000356164.4:n.*34G=
ENST00000427721.3:c.634+64G=
ENST00000429746.2:c.*34G=	ENSP00000402586.2:n.*34G=
ENST00000433655.6:c.*439G=	ENSP00000404902.1:n.*439G=
ENST00000438213.6:c.*34G=	ENSP00000415036.2:n.*34G=
ENST00000636397.1:c.1071+334G=	ENSP00000489910.1:n.1071+334G=
ENST00000636571.1:c.*34G=	ENSP00000490770.1:n.*34G=
ENST00000636579.1:c.72+334G=	ENSP00000490489.1:n.72+334G=
ENST00000636615.1:c.1071+334G=	ENSP00000490014.1:n.1071+334G=
ENST00000636843.1:c.*34G=	ENSP00000490897.1:n.*34G=
ENST00000637158.1:n.871G=
ENST00000637381.2:n.3701G=
ENST00000637387.1:c.*34G=	ENSP00000490598.1:n.*34G=
ENST00000637815.2:c.*34G=	ENSP00000490344.1:n.*34G=
ENST00000637915.1:c.*34G=	ENSP00000490471.1:n.*34G=
ENST00000637937.1:n.581G=
ENST00000678991.1:c.*1134G=	ENSP00000503019.1:n.*1134G=
ENST00000236671.6:c.*34G=	ENSP00000236671.2:n.*34G=
ENST00000427721.2:c.471+334G=	ENSP00000415840.2:n.471+334G=
ENST00000429746.1:c.604G=	ENSP00000402586.1:n.604G=
ENST00000433655.5:c.*439G=	ENSP00000404902.1:n.*439G=
NM_001909.4:c.*34G=	NP_001900.1:n.*34G=
NM_001909.5:c.*34G= MANE Select	NP_001900.1:n.*34G=