Canonical Allele Identifier: CA1947825305

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753893G= , CM000673.2:g.1753893G=	GRCh38
NC_000011.9:g.1775123G= , CM000673.1:g.1775123G=	GRCh37
NC_000011.8:g.1731699G=	NCBI36
NG_008655.1:g.15100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.981C= MANE Select	ENSP00000236671.2:p.Ile327=
ENST00000367196.4:c.876C=	ENSP00000356164.4:p.Ile292=
ENST00000427721.3:c.406C=
ENST00000429746.2:c.876C=	ENSP00000402586.2:p.Ile292=
ENST00000433655.6:c.*147C=	ENSP00000404902.1:n.*147C=
ENST00000438213.6:c.1098C=	ENSP00000415036.2:p.Ile366=
ENST00000497544.3:n.689C=
ENST00000636397.1:c.981C=	ENSP00000489910.1:p.Ile327=
ENST00000636571.1:c.960C=	ENSP00000490770.1:p.Ile320=
ENST00000636615.1:c.981C=	ENSP00000490014.1:p.Ile327=
ENST00000636843.1:c.975C=	ENSP00000490897.1:p.Ile325=
ENST00000637158.1:n.579C=
ENST00000637381.2:n.3409C=
ENST00000637387.1:c.973-13C=	ENSP00000490598.1:n.973-13C=
ENST00000637815.2:c.963C=	ENSP00000490344.1:p.Ile321=
ENST00000637915.1:c.981C=	ENSP00000490471.1:p.Ile327=
ENST00000637937.1:n.289C=
ENST00000678991.1:c.*842C=	ENSP00000503019.1:n.*842C=
ENST00000236671.6:c.981C=	ENSP00000236671.2:p.Ile327=
ENST00000427721.2:c.381C=	ENSP00000415840.2:p.Ile127=
ENST00000429746.1:c.312C=	ENSP00000402586.1:p.Ile104=
ENST00000433655.5:c.*147C=	ENSP00000404902.1:n.*147C=
ENST00000497544.1:n.689C=
NM_001909.4:c.981C=	NP_001900.1:p.Ile327=
NM_001909.5:c.981C= MANE Select	NP_001900.1:p.Ile327=