Canonical Allele Identifier: CA1947825270

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753819T= , CM000673.2:g.1753819T=	GRCh38
NC_000011.9:g.1775049T= , CM000673.1:g.1775049T=	GRCh37
NC_000011.8:g.1731625T=	NCBI36
NG_008655.1:g.15174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1055A= MANE Select	ENSP00000236671.2:p.Glu352=
ENST00000367196.4:c.950A=	ENSP00000356164.4:p.Glu317=
ENST00000427721.3:c.480A=
ENST00000429746.2:c.950A=	ENSP00000402586.2:p.Glu317=
ENST00000433655.6:c.*221A=	ENSP00000404902.1:n.*221A=
ENST00000438213.6:c.1172A=	ENSP00000415036.2:p.Glu391=
ENST00000497544.3:n.763A=
ENST00000636397.1:c.1055A=	ENSP00000489910.1:p.Glu352=
ENST00000636571.1:c.1034A=	ENSP00000490770.1:p.Glu345=
ENST00000636579.1:c.56A=	ENSP00000490489.1:p.Glu19=
ENST00000636615.1:c.1055A=	ENSP00000490014.1:p.Glu352=
ENST00000636843.1:c.1049A=	ENSP00000490897.1:p.Glu350=
ENST00000637158.1:n.653A=
ENST00000637381.2:n.3483A=
ENST00000637387.1:c.1034A=	ENSP00000490598.1:p.Glu345=
ENST00000637815.2:c.1037A=	ENSP00000490344.1:p.Glu346=
ENST00000637915.1:c.1055A=	ENSP00000490471.1:p.Glu352=
ENST00000637937.1:n.363A=
ENST00000678991.1:c.*916A=	ENSP00000503019.1:n.*916A=
ENST00000236671.6:c.1055A=	ENSP00000236671.2:p.Glu352=
ENST00000427721.2:c.455A=	ENSP00000415840.2:p.Glu152=
ENST00000429746.1:c.386A=	ENSP00000402586.1:p.Glu129=
ENST00000433655.5:c.*221A=	ENSP00000404902.1:n.*221A=
ENST00000497544.1:n.763A=
NM_001909.4:c.1055A=	NP_001900.1:p.Glu352=
NM_001909.5:c.1055A= MANE Select	NP_001900.1:p.Glu352=