Canonical Allele Identifier: CA1947825304

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753892G= , CM000673.2:g.1753892G=	GRCh38
NC_000011.9:g.1775122G= , CM000673.1:g.1775122G=	GRCh37
NC_000011.8:g.1731698G=	NCBI36
NG_008655.1:g.15101C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.982C= MANE Select	ENSP00000236671.2:p.Pro328=
ENST00000367196.4:c.877C=	ENSP00000356164.4:p.Pro293=
ENST00000427721.3:c.407C=
ENST00000429746.2:c.877C=	ENSP00000402586.2:p.Pro293=
ENST00000433655.6:c.*148C=	ENSP00000404902.1:n.*148C=
ENST00000438213.6:c.1099C=	ENSP00000415036.2:p.Pro367=
ENST00000497544.3:n.690C=
ENST00000636397.1:c.982C=	ENSP00000489910.1:p.Pro328=
ENST00000636571.1:c.961C=	ENSP00000490770.1:p.Pro321=
ENST00000636615.1:c.982C=	ENSP00000490014.1:p.Pro328=
ENST00000636843.1:c.976C=	ENSP00000490897.1:p.Pro326=
ENST00000637158.1:n.580C=
ENST00000637381.2:n.3410C=
ENST00000637387.1:c.973-12C=	ENSP00000490598.1:n.973-12C=
ENST00000637815.2:c.964C=	ENSP00000490344.1:p.Pro322=
ENST00000637915.1:c.982C=	ENSP00000490471.1:p.Pro328=
ENST00000637937.1:n.290C=
ENST00000678991.1:c.*843C=	ENSP00000503019.1:n.*843C=
ENST00000236671.6:c.982C=	ENSP00000236671.2:p.Pro328=
ENST00000427721.2:c.382C=	ENSP00000415840.2:p.Pro128=
ENST00000429746.1:c.313C=	ENSP00000402586.1:p.Pro105=
ENST00000433655.5:c.*148C=	ENSP00000404902.1:n.*148C=
ENST00000497544.1:n.690C=
NM_001909.4:c.982C=	NP_001900.1:p.Pro328=
NM_001909.5:c.982C= MANE Select	NP_001900.1:p.Pro328=