Canonical Allele Identifier: CA1947825400

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754049T= , CM000673.2:g.1754049T=	GRCh38
NC_000011.9:g.1775279T= , CM000673.1:g.1775279T=	GRCh37
NC_000011.8:g.1731855T=	NCBI36
NG_008655.1:g.14944A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.917A= MANE Select	ENSP00000236671.2:p.Asp306=
ENST00000367196.4:c.812A=	ENSP00000356164.4:p.Asp271=
ENST00000427721.3:c.342A=
ENST00000429746.2:c.812A=	ENSP00000402586.2:p.Asp271=
ENST00000433655.6:c.*83A=	ENSP00000404902.1:n.*83A=
ENST00000438213.6:c.1034A=	ENSP00000415036.2:p.Asp345=
ENST00000497544.3:n.533A=
ENST00000636397.1:c.917A=	ENSP00000489910.1:p.Asp306=
ENST00000636571.1:c.896A=	ENSP00000490770.1:p.Asp299=
ENST00000636615.1:c.917A=	ENSP00000490014.1:p.Asp306=
ENST00000636843.1:c.911A=	ENSP00000490897.1:p.Asp304=
ENST00000637158.1:n.515A=
ENST00000637381.2:n.3345A=
ENST00000637387.1:c.917A=	ENSP00000490598.1:p.Asp306=
ENST00000637815.2:c.899A=	ENSP00000490344.1:p.Asp300=
ENST00000637915.1:c.917A=	ENSP00000490471.1:p.Asp306=
ENST00000637937.1:n.225A=
ENST00000678991.1:c.*778A=	ENSP00000503019.1:n.*778A=
ENST00000236671.6:c.917A=	ENSP00000236671.2:p.Asp306=
ENST00000427721.2:c.317A=	ENSP00000415840.2:p.Asp106=
ENST00000429746.1:c.248A=	ENSP00000402586.1:p.Asp83=
ENST00000433655.5:c.*83A=	ENSP00000404902.1:n.*83A=
ENST00000438213.5:c.872A=	ENSP00000415036.1:p.Asp291=
ENST00000497544.1:n.533A=
NM_001909.4:c.917A=	NP_001900.1:p.Asp306=
NM_001909.5:c.917A= MANE Select	NP_001900.1:p.Asp306=