Canonical Allele Identifier: CA1947825121

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753574T= , CM000673.2:g.1753574T=	GRCh38
NC_000011.9:g.1774804T= , CM000673.1:g.1774804T=	GRCh37
NC_000011.8:g.1731380T=	NCBI36
NG_008655.1:g.15419A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1168A= MANE Select	ENSP00000236671.2:p.Ile390=
ENST00000367196.4:c.1063A=	ENSP00000356164.4:p.Ile355=
ENST00000427721.3:c.593A=
ENST00000429746.2:c.1063A=	ENSP00000402586.2:p.Ile355=
ENST00000433655.6:c.*334A=	ENSP00000404902.1:n.*334A=
ENST00000438213.6:c.1285A=	ENSP00000415036.2:p.Ile429=
ENST00000636397.1:c.1071+229A=	ENSP00000489910.1:n.1071+229A=
ENST00000636571.1:c.1147A=	ENSP00000490770.1:p.Ile383=
ENST00000636579.1:c.72+229A=	ENSP00000490489.1:n.72+229A=
ENST00000636615.1:c.1071+229A=	ENSP00000490014.1:n.1071+229A=
ENST00000636843.1:c.1162A=	ENSP00000490897.1:p.Ile388=
ENST00000637158.1:n.766A=
ENST00000637381.2:n.3596A=
ENST00000637387.1:c.1147A=	ENSP00000490598.1:p.Ile383=
ENST00000637815.2:c.1150A=	ENSP00000490344.1:p.Ile384=
ENST00000637915.1:c.1159A=	ENSP00000490471.1:p.Ile387=
ENST00000637937.1:n.476A=
ENST00000678991.1:c.*1029A=	ENSP00000503019.1:n.*1029A=
ENST00000236671.6:c.1168A=	ENSP00000236671.2:p.Ile390=
ENST00000427721.2:c.471+229A=	ENSP00000415840.2:n.471+229A=
ENST00000429746.1:c.499A=	ENSP00000402586.1:p.Ile167=
ENST00000433655.5:c.*334A=	ENSP00000404902.1:n.*334A=
NM_001909.4:c.1168A=	NP_001900.1:p.Ile390=
NM_001909.5:c.1168A= MANE Select	NP_001900.1:p.Ile390=