Canonical Allele Identifier: CA1947825164

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753666G= , CM000673.2:g.1753666G=	GRCh38
NC_000011.9:g.1774896G= , CM000673.1:g.1774896G=	GRCh37
NC_000011.8:g.1731472G=	NCBI36
NG_008655.1:g.15327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1076C= MANE Select	ENSP00000236671.2:p.Ser359=
ENST00000367196.4:c.971C=	ENSP00000356164.4:p.Ser324=
ENST00000427721.3:c.501C=
ENST00000429746.2:c.971C=	ENSP00000402586.2:p.Ser324=
ENST00000433655.6:c.*242C=	ENSP00000404902.1:n.*242C=
ENST00000438213.6:c.1193C=	ENSP00000415036.2:p.Ser398=
ENST00000497544.3:n.784C=
ENST00000636397.1:c.1071+137C=	ENSP00000489910.1:n.1071+137C=
ENST00000636571.1:c.1055C=	ENSP00000490770.1:p.Ser352=
ENST00000636579.1:c.72+137C=	ENSP00000490489.1:n.72+137C=
ENST00000636615.1:c.1071+137C=	ENSP00000490014.1:n.1071+137C=
ENST00000636843.1:c.1070C=	ENSP00000490897.1:p.Ser357=
ENST00000637158.1:n.674C=
ENST00000637381.2:n.3504C=
ENST00000637387.1:c.1055C=	ENSP00000490598.1:p.Ser352=
ENST00000637815.2:c.1058C=	ENSP00000490344.1:p.Ser353=
ENST00000637915.1:c.1072-5C=	ENSP00000490471.1:n.1072-5C=
ENST00000637937.1:n.384C=
ENST00000678991.1:c.*937C=	ENSP00000503019.1:n.*937C=
ENST00000236671.6:c.1076C=	ENSP00000236671.2:p.Ser359=
ENST00000427721.2:c.471+137C=	ENSP00000415840.2:n.471+137C=
ENST00000429746.1:c.407C=	ENSP00000402586.1:p.Ser136=
ENST00000433655.5:c.*242C=	ENSP00000404902.1:n.*242C=
NM_001909.4:c.1076C=	NP_001900.1:p.Ser359=
NM_001909.5:c.1076C= MANE Select	NP_001900.1:p.Ser359=