Canonical Allele Identifier: CA1947825154

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753638G= , CM000673.2:g.1753638G=	GRCh38
NC_000011.9:g.1774868G= , CM000673.1:g.1774868G=	GRCh37
NC_000011.8:g.1731444G=	NCBI36
NG_008655.1:g.15355C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1104C= MANE Select	ENSP00000236671.2:p.Ser368=
ENST00000367196.4:c.999C=	ENSP00000356164.4:p.Ser333=
ENST00000427721.3:c.529C=
ENST00000429746.2:c.999C=	ENSP00000402586.2:p.Ser333=
ENST00000433655.6:c.*270C=	ENSP00000404902.1:n.*270C=
ENST00000438213.6:c.1221C=	ENSP00000415036.2:p.Ser407=
ENST00000636397.1:c.1071+165C=	ENSP00000489910.1:n.1071+165C=
ENST00000636571.1:c.1083C=	ENSP00000490770.1:p.Ser361=
ENST00000636579.1:c.72+165C=	ENSP00000490489.1:n.72+165C=
ENST00000636615.1:c.1071+165C=	ENSP00000490014.1:n.1071+165C=
ENST00000636843.1:c.1098C=	ENSP00000490897.1:p.Ser366=
ENST00000637158.1:n.702C=
ENST00000637381.2:n.3532C=
ENST00000637387.1:c.1083C=	ENSP00000490598.1:p.Ser361=
ENST00000637815.2:c.1086C=	ENSP00000490344.1:p.Ser362=
ENST00000637915.1:c.1095C=	ENSP00000490471.1:p.Ser365=
ENST00000637937.1:n.412C=
ENST00000678991.1:c.*965C=	ENSP00000503019.1:n.*965C=
ENST00000236671.6:c.1104C=	ENSP00000236671.2:p.Ser368=
ENST00000427721.2:c.471+165C=	ENSP00000415840.2:n.471+165C=
ENST00000429746.1:c.435C=	ENSP00000402586.1:p.Ser145=
ENST00000433655.5:c.*270C=	ENSP00000404902.1:n.*270C=
NM_001909.4:c.1104C=	NP_001900.1:p.Ser368=
NM_001909.5:c.1104C= MANE Select	NP_001900.1:p.Ser368=