Canonical Allele Identifier: CA1947825053

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753454C= , CM000673.2:g.1753454C=	GRCh38
NC_000011.9:g.1774684C= , CM000673.1:g.1774684C=	GRCh37
NC_000011.8:g.1731260C=	NCBI36
NG_008655.1:g.15539G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*49G= MANE Select	ENSP00000236671.2:n.*49G=
ENST00000367196.4:c.*49G=	ENSP00000356164.4:n.*49G=
ENST00000427721.3:c.634+79G=
ENST00000429746.2:c.*49G=	ENSP00000402586.2:n.*49G=
ENST00000433655.6:c.*454G=	ENSP00000404902.1:n.*454G=
ENST00000438213.6:c.*49G=	ENSP00000415036.2:n.*49G=
ENST00000636397.1:c.1071+349G=	ENSP00000489910.1:n.1071+349G=
ENST00000636571.1:c.*49G=	ENSP00000490770.1:n.*49G=
ENST00000636579.1:c.72+349G=	ENSP00000490489.1:n.72+349G=
ENST00000636615.1:c.1071+349G=	ENSP00000490014.1:n.1071+349G=
ENST00000636843.1:c.*49G=	ENSP00000490897.1:n.*49G=
ENST00000637158.1:n.886G=
ENST00000637381.2:n.3716G=
ENST00000637387.1:c.*49G=	ENSP00000490598.1:n.*49G=
ENST00000637815.2:c.*49G=	ENSP00000490344.1:n.*49G=
ENST00000637915.1:c.*49G=	ENSP00000490471.1:n.*49G=
ENST00000637937.1:n.596G=
ENST00000678991.1:c.*1149G=	ENSP00000503019.1:n.*1149G=
ENST00000236671.6:c.*49G=	ENSP00000236671.2:n.*49G=
ENST00000427721.2:c.471+349G=	ENSP00000415840.2:n.471+349G=
ENST00000429746.1:c.619G=	ENSP00000402586.1:n.619G=
ENST00000433655.5:c.*454G=	ENSP00000404902.1:n.*454G=
NM_001909.4:c.*49G=	NP_001900.1:n.*49G=
NM_001909.5:c.*49G= MANE Select	NP_001900.1:n.*49G=