Canonical Allele Identifier: CA1947825395

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754038C= , CM000673.2:g.1754038C=	GRCh38
NC_000011.9:g.1775268C= , CM000673.1:g.1775268C=	GRCh37
NC_000011.8:g.1731844C=	NCBI36
NG_008655.1:g.14955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.928G= MANE Select	ENSP00000236671.2:p.Glu310=
ENST00000367196.4:c.823G=	ENSP00000356164.4:p.Glu275=
ENST00000427721.3:c.353G=
ENST00000429746.2:c.823G=	ENSP00000402586.2:p.Glu275=
ENST00000433655.6:c.*94G=	ENSP00000404902.1:n.*94G=
ENST00000438213.6:c.1045G=	ENSP00000415036.2:p.Glu349=
ENST00000497544.3:n.544G=
ENST00000636397.1:c.928G=	ENSP00000489910.1:p.Glu310=
ENST00000636571.1:c.907G=	ENSP00000490770.1:p.Glu303=
ENST00000636615.1:c.928G=	ENSP00000490014.1:p.Glu310=
ENST00000636843.1:c.922G=	ENSP00000490897.1:p.Glu308=
ENST00000637158.1:n.526G=
ENST00000637381.2:n.3356G=
ENST00000637387.1:c.928G=	ENSP00000490598.1:p.Glu310=
ENST00000637815.2:c.910G=	ENSP00000490344.1:p.Glu304=
ENST00000637915.1:c.928G=	ENSP00000490471.1:p.Glu310=
ENST00000637937.1:n.236G=
ENST00000678991.1:c.*789G=	ENSP00000503019.1:n.*789G=
ENST00000236671.6:c.928G=	ENSP00000236671.2:p.Glu310=
ENST00000427721.2:c.328G=	ENSP00000415840.2:p.Glu110=
ENST00000429746.1:c.259G=	ENSP00000402586.1:p.Glu87=
ENST00000433655.5:c.*94G=	ENSP00000404902.1:n.*94G=
ENST00000438213.5:c.883G=	ENSP00000415036.1:p.Glu295=
ENST00000497544.1:n.544G=
NM_001909.4:c.928G=	NP_001900.1:p.Glu310=
NM_001909.5:c.928G= MANE Select	NP_001900.1:p.Glu310=