Canonical Allele Identifier: CA1947825098

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753524G= , CM000673.2:g.1753524G=	GRCh38
NC_000011.9:g.1774754G= , CM000673.1:g.1774754G=	GRCh37
NC_000011.8:g.1731330G=	NCBI36
NG_008655.1:g.15469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1218C= MANE Select	ENSP00000236671.2:p.Phe406=
ENST00000367196.4:c.1113C=	ENSP00000356164.4:p.Phe371=
ENST00000427721.3:c.634+9C=
ENST00000429746.2:c.1113C=	ENSP00000402586.2:p.Phe371=
ENST00000433655.6:c.*384C=	ENSP00000404902.1:n.*384C=
ENST00000438213.6:c.1335C=	ENSP00000415036.2:p.Phe445=
ENST00000636397.1:c.1071+279C=	ENSP00000489910.1:n.1071+279C=
ENST00000636571.1:c.1197C=	ENSP00000490770.1:p.Phe399=
ENST00000636579.1:c.72+279C=	ENSP00000490489.1:n.72+279C=
ENST00000636615.1:c.1071+279C=	ENSP00000490014.1:n.1071+279C=
ENST00000636843.1:c.1212C=	ENSP00000490897.1:p.Phe404=
ENST00000637158.1:n.816C=
ENST00000637381.2:n.3646C=
ENST00000637387.1:c.1197C=	ENSP00000490598.1:p.Phe399=
ENST00000637815.2:c.1200C=	ENSP00000490344.1:p.Phe400=
ENST00000637915.1:c.1209C=	ENSP00000490471.1:p.Phe403=
ENST00000637937.1:n.526C=
ENST00000678991.1:c.*1079C=	ENSP00000503019.1:n.*1079C=
ENST00000236671.6:c.1218C=	ENSP00000236671.2:p.Phe406=
ENST00000427721.2:c.471+279C=	ENSP00000415840.2:n.471+279C=
ENST00000429746.1:c.549C=	ENSP00000402586.1:p.Phe183=
ENST00000433655.5:c.*384C=	ENSP00000404902.1:n.*384C=
NM_001909.4:c.1218C=	NP_001900.1:p.Phe406=
NM_001909.5:c.1218C= MANE Select	NP_001900.1:p.Phe406=