Canonical Allele Identifier: CA1947825104

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753534C= , CM000673.2:g.1753534C=	GRCh38
NC_000011.9:g.1774764C= , CM000673.1:g.1774764C=	GRCh37
NC_000011.8:g.1731340C=	NCBI36
NG_008655.1:g.15459G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1208G= MANE Select	ENSP00000236671.2:p.Arg403=
ENST00000367196.4:c.1103G=	ENSP00000356164.4:p.Arg368=
ENST00000427721.3:c.633G=
ENST00000429746.2:c.1103G=	ENSP00000402586.2:p.Arg368=
ENST00000433655.6:c.*374G=	ENSP00000404902.1:n.*374G=
ENST00000438213.6:c.1325G=	ENSP00000415036.2:p.Arg442=
ENST00000636397.1:c.1071+269G=	ENSP00000489910.1:n.1071+269G=
ENST00000636571.1:c.1187G=	ENSP00000490770.1:p.Arg396=
ENST00000636579.1:c.72+269G=	ENSP00000490489.1:n.72+269G=
ENST00000636615.1:c.1071+269G=	ENSP00000490014.1:n.1071+269G=
ENST00000636843.1:c.1202G=	ENSP00000490897.1:p.Arg401=
ENST00000637158.1:n.806G=
ENST00000637381.2:n.3636G=
ENST00000637387.1:c.1187G=	ENSP00000490598.1:p.Arg396=
ENST00000637815.2:c.1190G=	ENSP00000490344.1:p.Arg397=
ENST00000637915.1:c.1199G=	ENSP00000490471.1:p.Arg400=
ENST00000637937.1:n.516G=
ENST00000678991.1:c.*1069G=	ENSP00000503019.1:n.*1069G=
ENST00000236671.6:c.1208G=	ENSP00000236671.2:p.Arg403=
ENST00000427721.2:c.471+269G=	ENSP00000415840.2:n.471+269G=
ENST00000429746.1:c.539G=	ENSP00000402586.1:p.Arg180=
ENST00000433655.5:c.*374G=	ENSP00000404902.1:n.*374G=
NM_001909.4:c.1208G=	NP_001900.1:p.Arg403=
NM_001909.5:c.1208G= MANE Select	NP_001900.1:p.Arg403=