Canonical Allele Identifier: CA1947825397

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754040C= , CM000673.2:g.1754040C=	GRCh38
NC_000011.9:g.1775270C= , CM000673.1:g.1775270C=	GRCh37
NC_000011.8:g.1731846C=	NCBI36
NG_008655.1:g.14953G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.926G= MANE Select	ENSP00000236671.2:p.Arg309=
ENST00000367196.4:c.821G=	ENSP00000356164.4:p.Arg274=
ENST00000427721.3:c.351G=
ENST00000429746.2:c.821G=	ENSP00000402586.2:p.Arg274=
ENST00000433655.6:c.*92G=	ENSP00000404902.1:n.*92G=
ENST00000438213.6:c.1043G=	ENSP00000415036.2:p.Arg348=
ENST00000497544.3:n.542G=
ENST00000636397.1:c.926G=	ENSP00000489910.1:p.Arg309=
ENST00000636571.1:c.905G=	ENSP00000490770.1:p.Arg302=
ENST00000636615.1:c.926G=	ENSP00000490014.1:p.Arg309=
ENST00000636843.1:c.920G=	ENSP00000490897.1:p.Arg307=
ENST00000637158.1:n.524G=
ENST00000637381.2:n.3354G=
ENST00000637387.1:c.926G=	ENSP00000490598.1:p.Arg309=
ENST00000637815.2:c.908G=	ENSP00000490344.1:p.Arg303=
ENST00000637915.1:c.926G=	ENSP00000490471.1:p.Arg309=
ENST00000637937.1:n.234G=
ENST00000678991.1:c.*787G=	ENSP00000503019.1:n.*787G=
ENST00000236671.6:c.926G=	ENSP00000236671.2:p.Arg309=
ENST00000427721.2:c.326G=	ENSP00000415840.2:p.Arg109=
ENST00000429746.1:c.257G=	ENSP00000402586.1:p.Arg86=
ENST00000433655.5:c.*92G=	ENSP00000404902.1:n.*92G=
ENST00000438213.5:c.881G=	ENSP00000415036.1:p.Arg294=
ENST00000497544.1:n.542G=
NM_001909.4:c.926G=	NP_001900.1:p.Arg309=
NM_001909.5:c.926G= MANE Select	NP_001900.1:p.Arg309=