Canonical Allele Identifier: CA1947825150

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753629C= , CM000673.2:g.1753629C=	GRCh38
NC_000011.9:g.1774859C= , CM000673.1:g.1774859C=	GRCh37
NC_000011.8:g.1731435C=	NCBI36
NG_008655.1:g.15364G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1113G= MANE Select	ENSP00000236671.2:p.Met371=
ENST00000367196.4:c.1008G=	ENSP00000356164.4:p.Met336=
ENST00000427721.3:c.538G=
ENST00000429746.2:c.1008G=	ENSP00000402586.2:p.Met336=
ENST00000433655.6:c.*279G=	ENSP00000404902.1:n.*279G=
ENST00000438213.6:c.1230G=	ENSP00000415036.2:p.Met410=
ENST00000636397.1:c.1071+174G=	ENSP00000489910.1:n.1071+174G=
ENST00000636571.1:c.1092G=	ENSP00000490770.1:p.Met364=
ENST00000636579.1:c.72+174G=	ENSP00000490489.1:n.72+174G=
ENST00000636615.1:c.1071+174G=	ENSP00000490014.1:n.1071+174G=
ENST00000636843.1:c.1107G=	ENSP00000490897.1:p.Met369=
ENST00000637158.1:n.711G=
ENST00000637381.2:n.3541G=
ENST00000637387.1:c.1092G=	ENSP00000490598.1:p.Met364=
ENST00000637815.2:c.1095G=	ENSP00000490344.1:p.Met365=
ENST00000637915.1:c.1104G=	ENSP00000490471.1:p.Met368=
ENST00000637937.1:n.421G=
ENST00000678991.1:c.*974G=	ENSP00000503019.1:n.*974G=
ENST00000236671.6:c.1113G=	ENSP00000236671.2:p.Met371=
ENST00000427721.2:c.471+174G=	ENSP00000415840.2:n.471+174G=
ENST00000429746.1:c.444G=	ENSP00000402586.1:p.Met148=
ENST00000433655.5:c.*279G=	ENSP00000404902.1:n.*279G=
NM_001909.4:c.1113G=	NP_001900.1:p.Met371=
NM_001909.5:c.1113G= MANE Select	NP_001900.1:p.Met371=