Canonical Allele Identifier: CA1947826317

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754982C= , CM000673.2:g.1754982C=	GRCh38
NC_000011.9:g.1776212C= , CM000673.1:g.1776212C=	GRCh37
NC_000011.8:g.1732788C=	NCBI36
NG_008655.1:g.14011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.751G= MANE Select	ENSP00000236671.2:p.Asp251=
ENST00000367196.4:c.646G=	ENSP00000356164.4:p.Asp216=
ENST00000427721.3:c.176G=
ENST00000429746.2:c.646G=	ENSP00000402586.2:p.Asp216=
ENST00000433655.6:c.751G=	ENSP00000404902.1:p.Asp251=
ENST00000438213.6:c.751G=	ENSP00000415036.2:p.Asp251=
ENST00000497544.3:n.367G=
ENST00000636397.1:c.751G=	ENSP00000489910.1:p.Asp251=
ENST00000636571.1:c.730G=	ENSP00000490770.1:p.Asp244=
ENST00000636615.1:c.751G=	ENSP00000490014.1:p.Asp251=
ENST00000636843.1:c.745G=	ENSP00000490897.1:p.Asp249=
ENST00000637158.1:n.349G=
ENST00000637381.2:n.3179G=
ENST00000637387.1:c.751G=	ENSP00000490598.1:p.Asp251=
ENST00000637815.2:c.751G=	ENSP00000490344.1:p.Asp251=
ENST00000637915.1:c.751G=	ENSP00000490471.1:p.Asp251=
ENST00000637937.1:n.59G=
ENST00000678991.1:c.*612G=	ENSP00000503019.1:n.*612G=
ENST00000236671.6:c.751G=	ENSP00000236671.2:p.Asp251=
ENST00000427721.2:c.151G=	ENSP00000415840.2:p.Asp51=
ENST00000433655.5:c.751G=	ENSP00000404902.1:p.Asp251=
ENST00000438213.5:c.706G=	ENSP00000415036.1:p.Asp236=
ENST00000497544.1:n.367G=
NM_001909.4:c.751G=	NP_001900.1:p.Asp251=
NM_001909.5:c.751G= MANE Select	NP_001900.1:p.Asp251=