Canonical Allele Identifier: CA1947825401

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754050C= , CM000673.2:g.1754050C=	GRCh38
NC_000011.9:g.1775280C= , CM000673.1:g.1775280C=	GRCh37
NC_000011.8:g.1731856C=	NCBI36
NG_008655.1:g.14943G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.916G= MANE Select	ENSP00000236671.2:p.Asp306=
ENST00000367196.4:c.811G=	ENSP00000356164.4:p.Asp271=
ENST00000427721.3:c.341G=
ENST00000429746.2:c.811G=	ENSP00000402586.2:p.Asp271=
ENST00000433655.6:c.*82G=	ENSP00000404902.1:n.*82G=
ENST00000438213.6:c.1033G=	ENSP00000415036.2:p.Asp345=
ENST00000497544.3:n.532G=
ENST00000636397.1:c.916G=	ENSP00000489910.1:p.Asp306=
ENST00000636571.1:c.895G=	ENSP00000490770.1:p.Asp299=
ENST00000636615.1:c.916G=	ENSP00000490014.1:p.Asp306=
ENST00000636843.1:c.910G=	ENSP00000490897.1:p.Asp304=
ENST00000637158.1:n.514G=
ENST00000637381.2:n.3344G=
ENST00000637387.1:c.916G=	ENSP00000490598.1:p.Asp306=
ENST00000637815.2:c.898G=	ENSP00000490344.1:p.Asp300=
ENST00000637915.1:c.916G=	ENSP00000490471.1:p.Asp306=
ENST00000637937.1:n.224G=
ENST00000678991.1:c.*777G=	ENSP00000503019.1:n.*777G=
ENST00000236671.6:c.916G=	ENSP00000236671.2:p.Asp306=
ENST00000427721.2:c.316G=	ENSP00000415840.2:p.Asp106=
ENST00000429746.1:c.247G=	ENSP00000402586.1:p.Asp83=
ENST00000433655.5:c.*82G=	ENSP00000404902.1:n.*82G=
ENST00000438213.5:c.871G=	ENSP00000415036.1:p.Asp291=
ENST00000497544.1:n.532G=
NM_001909.4:c.916G=	NP_001900.1:p.Asp306=
NM_001909.5:c.916G= MANE Select	NP_001900.1:p.Asp306=