Canonical Allele Identifier: CA1947825152

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753631T= , CM000673.2:g.1753631T=	GRCh38
NC_000011.9:g.1774861T= , CM000673.1:g.1774861T=	GRCh37
NC_000011.8:g.1731437T=	NCBI36
NG_008655.1:g.15362A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1111A= MANE Select	ENSP00000236671.2:p.Met371=
ENST00000367196.4:c.1006A=	ENSP00000356164.4:p.Met336=
ENST00000427721.3:c.536A=
ENST00000429746.2:c.1006A=	ENSP00000402586.2:p.Met336=
ENST00000433655.6:c.*277A=	ENSP00000404902.1:n.*277A=
ENST00000438213.6:c.1228A=	ENSP00000415036.2:p.Met410=
ENST00000636397.1:c.1071+172A=	ENSP00000489910.1:n.1071+172A=
ENST00000636571.1:c.1090A=	ENSP00000490770.1:p.Met364=
ENST00000636579.1:c.72+172A=	ENSP00000490489.1:n.72+172A=
ENST00000636615.1:c.1071+172A=	ENSP00000490014.1:n.1071+172A=
ENST00000636843.1:c.1105A=	ENSP00000490897.1:p.Met369=
ENST00000637158.1:n.709A=
ENST00000637381.2:n.3539A=
ENST00000637387.1:c.1090A=	ENSP00000490598.1:p.Met364=
ENST00000637815.2:c.1093A=	ENSP00000490344.1:p.Met365=
ENST00000637915.1:c.1102A=	ENSP00000490471.1:p.Met368=
ENST00000637937.1:n.419A=
ENST00000678991.1:c.*972A=	ENSP00000503019.1:n.*972A=
ENST00000236671.6:c.1111A=	ENSP00000236671.2:p.Met371=
ENST00000427721.2:c.471+172A=	ENSP00000415840.2:n.471+172A=
ENST00000429746.1:c.442A=	ENSP00000402586.1:p.Met148=
ENST00000433655.5:c.*277A=	ENSP00000404902.1:n.*277A=
NM_001909.4:c.1111A=	NP_001900.1:p.Met371=
NM_001909.5:c.1111A= MANE Select	NP_001900.1:p.Met371=