Canonical Allele Identifier: CA1947825387

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754023T= , CM000673.2:g.1754023T=	GRCh38
NC_000011.9:g.1775253T= , CM000673.1:g.1775253T=	GRCh37
NC_000011.8:g.1731829T=	NCBI36
NG_008655.1:g.14970A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.943A= MANE Select	ENSP00000236671.2:p.Ile315=
ENST00000367196.4:c.838A=	ENSP00000356164.4:p.Ile280=
ENST00000427721.3:c.368A=
ENST00000429746.2:c.838A=	ENSP00000402586.2:p.Ile280=
ENST00000433655.6:c.*109A=	ENSP00000404902.1:n.*109A=
ENST00000438213.6:c.1060A=	ENSP00000415036.2:p.Ile354=
ENST00000497544.3:n.559A=
ENST00000636397.1:c.943A=	ENSP00000489910.1:p.Ile315=
ENST00000636571.1:c.922A=	ENSP00000490770.1:p.Ile308=
ENST00000636615.1:c.943A=	ENSP00000490014.1:p.Ile315=
ENST00000636843.1:c.937A=	ENSP00000490897.1:p.Ile313=
ENST00000637158.1:n.541A=
ENST00000637381.2:n.3371A=
ENST00000637387.1:c.943A=	ENSP00000490598.1:p.Ile315=
ENST00000637815.2:c.925A=	ENSP00000490344.1:p.Ile309=
ENST00000637915.1:c.943A=	ENSP00000490471.1:p.Ile315=
ENST00000637937.1:n.251A=
ENST00000678991.1:c.*804A=	ENSP00000503019.1:n.*804A=
ENST00000236671.6:c.943A=	ENSP00000236671.2:p.Ile315=
ENST00000427721.2:c.343A=	ENSP00000415840.2:p.Ile115=
ENST00000429746.1:c.274A=	ENSP00000402586.1:p.Ile92=
ENST00000433655.5:c.*109A=	ENSP00000404902.1:n.*109A=
ENST00000497544.1:n.559A=
NM_001909.4:c.943A=	NP_001900.1:p.Ile315=
NM_001909.5:c.943A= MANE Select	NP_001900.1:p.Ile315=