Canonical Allele Identifier: CA1947834676

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759554A= , CM000673.2:g.1759554A=	GRCh38
NC_000011.9:g.1780784A= , CM000673.1:g.1780784A=	GRCh37
NC_000011.8:g.1737360A=	NCBI36
NG_008655.1:g.9439T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.314T= MANE Select	ENSP00000236671.2:p.Val105=
ENST00000367196.4:c.209T=	ENSP00000356164.4:p.Val70=
ENST00000429746.2:c.209T=	ENSP00000402586.2:p.Val70=
ENST00000433655.6:c.314T=	ENSP00000404902.1:p.Val105=
ENST00000438213.6:c.314T=	ENSP00000415036.2:p.Val105=
ENST00000636397.1:c.314T=	ENSP00000489910.1:p.Val105=
ENST00000636571.1:c.293T=	ENSP00000490770.1:p.Val98=
ENST00000636615.1:c.314T=	ENSP00000490014.1:p.Val105=
ENST00000636843.1:c.308T=	ENSP00000490897.1:p.Val103=
ENST00000637381.2:n.2742T=
ENST00000637387.1:c.314T=	ENSP00000490598.1:p.Val105=
ENST00000637815.2:c.314T=	ENSP00000490344.1:p.Val105=
ENST00000637915.1:c.314T=	ENSP00000490471.1:p.Val105=
ENST00000677300.1:n.709T=
ENST00000678991.1:c.*175T=	ENSP00000503019.1:n.*175T=
ENST00000236671.6:c.314T=	ENSP00000236671.2:p.Val105=
ENST00000367196.3:c.209T=	ENSP00000356164.3:p.Val70=
ENST00000433655.5:c.314T=	ENSP00000404902.1:p.Val105=
ENST00000438213.5:c.269T=	ENSP00000415036.1:p.Val90=
NM_001909.4:c.314T=	NP_001900.1:p.Val105=
NM_001909.5:c.314T= MANE Select	NP_001900.1:p.Val105=