Canonical Allele Identifier: CA1947825306

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753896C= , CM000673.2:g.1753896C=	GRCh38
NC_000011.9:g.1775126C= , CM000673.1:g.1775126C=	GRCh37
NC_000011.8:g.1731702C=	NCBI36
NG_008655.1:g.15097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.978G= MANE Select	ENSP00000236671.2:p.Met326=
ENST00000367196.4:c.873G=	ENSP00000356164.4:p.Met291=
ENST00000427721.3:c.403G=
ENST00000429746.2:c.873G=	ENSP00000402586.2:p.Met291=
ENST00000433655.6:c.*144G=	ENSP00000404902.1:n.*144G=
ENST00000438213.6:c.1095G=	ENSP00000415036.2:p.Met365=
ENST00000497544.3:n.686G=
ENST00000636397.1:c.978G=	ENSP00000489910.1:p.Met326=
ENST00000636571.1:c.957G=	ENSP00000490770.1:p.Met319=
ENST00000636615.1:c.978G=	ENSP00000490014.1:p.Met326=
ENST00000636843.1:c.972G=	ENSP00000490897.1:p.Met324=
ENST00000637158.1:n.576G=
ENST00000637381.2:n.3406G=
ENST00000637387.1:c.973-16G=	ENSP00000490598.1:n.973-16G=
ENST00000637815.2:c.960G=	ENSP00000490344.1:p.Met320=
ENST00000637915.1:c.978G=	ENSP00000490471.1:p.Met326=
ENST00000637937.1:n.286G=
ENST00000678991.1:c.*839G=	ENSP00000503019.1:n.*839G=
ENST00000236671.6:c.978G=	ENSP00000236671.2:p.Met326=
ENST00000427721.2:c.378G=	ENSP00000415840.2:p.Met126=
ENST00000429746.1:c.309G=	ENSP00000402586.1:p.Met103=
ENST00000433655.5:c.*144G=	ENSP00000404902.1:n.*144G=
ENST00000497544.1:n.686G=
NM_001909.4:c.978G=	NP_001900.1:p.Met326=
NM_001909.5:c.978G= MANE Select	NP_001900.1:p.Met326=