Canonical Allele Identifier: CA1947825399

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754042C= , CM000673.2:g.1754042C=	GRCh38
NC_000011.9:g.1775272C= , CM000673.1:g.1775272C=	GRCh37
NC_000011.8:g.1731848C=	NCBI36
NG_008655.1:g.14951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.924G= MANE Select	ENSP00000236671.2:p.Val308=
ENST00000367196.4:c.819G=	ENSP00000356164.4:p.Val273=
ENST00000427721.3:c.349G=
ENST00000429746.2:c.819G=	ENSP00000402586.2:p.Val273=
ENST00000433655.6:c.*90G=	ENSP00000404902.1:n.*90G=
ENST00000438213.6:c.1041G=	ENSP00000415036.2:p.Val347=
ENST00000497544.3:n.540G=
ENST00000636397.1:c.924G=	ENSP00000489910.1:p.Val308=
ENST00000636571.1:c.903G=	ENSP00000490770.1:p.Val301=
ENST00000636615.1:c.924G=	ENSP00000490014.1:p.Val308=
ENST00000636843.1:c.918G=	ENSP00000490897.1:p.Val306=
ENST00000637158.1:n.522G=
ENST00000637381.2:n.3352G=
ENST00000637387.1:c.924G=	ENSP00000490598.1:p.Val308=
ENST00000637815.2:c.906G=	ENSP00000490344.1:p.Val302=
ENST00000637915.1:c.924G=	ENSP00000490471.1:p.Val308=
ENST00000637937.1:n.232G=
ENST00000678991.1:c.*785G=	ENSP00000503019.1:n.*785G=
ENST00000236671.6:c.924G=	ENSP00000236671.2:p.Val308=
ENST00000427721.2:c.324G=	ENSP00000415840.2:p.Val108=
ENST00000429746.1:c.255G=	ENSP00000402586.1:p.Val85=
ENST00000433655.5:c.*90G=	ENSP00000404902.1:n.*90G=
ENST00000438213.5:c.879G=	ENSP00000415036.1:p.Val293=
ENST00000497544.1:n.540G=
NM_001909.4:c.924G=	NP_001900.1:p.Val308=
NM_001909.5:c.924G= MANE Select	NP_001900.1:p.Val308=