Canonical Allele Identifier: CA1947825273

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753823G= , CM000673.2:g.1753823G=	GRCh38
NC_000011.9:g.1775053G= , CM000673.1:g.1775053G=	GRCh37
NC_000011.8:g.1731629G=	NCBI36
NG_008655.1:g.15170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1051C= MANE Select	ENSP00000236671.2:p.Pro351=
ENST00000367196.4:c.946C=	ENSP00000356164.4:p.Pro316=
ENST00000427721.3:c.476C=
ENST00000429746.2:c.946C=	ENSP00000402586.2:p.Pro316=
ENST00000433655.6:c.*217C=	ENSP00000404902.1:n.*217C=
ENST00000438213.6:c.1168C=	ENSP00000415036.2:p.Pro390=
ENST00000497544.3:n.759C=
ENST00000636397.1:c.1051C=	ENSP00000489910.1:p.Pro351=
ENST00000636571.1:c.1030C=	ENSP00000490770.1:p.Pro344=
ENST00000636579.1:c.52C=	ENSP00000490489.1:p.Pro18=
ENST00000636615.1:c.1051C=	ENSP00000490014.1:p.Pro351=
ENST00000636843.1:c.1045C=	ENSP00000490897.1:p.Pro349=
ENST00000637158.1:n.649C=
ENST00000637381.2:n.3479C=
ENST00000637387.1:c.1030C=	ENSP00000490598.1:p.Pro344=
ENST00000637815.2:c.1033C=	ENSP00000490344.1:p.Pro345=
ENST00000637915.1:c.1051C=	ENSP00000490471.1:p.Pro351=
ENST00000637937.1:n.359C=
ENST00000678991.1:c.*912C=	ENSP00000503019.1:n.*912C=
ENST00000236671.6:c.1051C=	ENSP00000236671.2:p.Pro351=
ENST00000427721.2:c.451C=	ENSP00000415840.2:p.Pro151=
ENST00000429746.1:c.382C=	ENSP00000402586.1:p.Pro128=
ENST00000433655.5:c.*217C=	ENSP00000404902.1:n.*217C=
ENST00000497544.1:n.759C=
NM_001909.4:c.1051C=	NP_001900.1:p.Pro351=
NM_001909.5:c.1051C= MANE Select	NP_001900.1:p.Pro351=