Canonical Allele Identifier: CA1947825277

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753837C= , CM000673.2:g.1753837C=	GRCh38
NC_000011.9:g.1775067C= , CM000673.1:g.1775067C=	GRCh37
NC_000011.8:g.1731643C=	NCBI36
NG_008655.1:g.15156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1037G= MANE Select	ENSP00000236671.2:p.Gly346=
ENST00000367196.4:c.932G=	ENSP00000356164.4:p.Gly311=
ENST00000427721.3:c.462G=
ENST00000429746.2:c.932G=	ENSP00000402586.2:p.Gly311=
ENST00000433655.6:c.*203G=	ENSP00000404902.1:n.*203G=
ENST00000438213.6:c.1154G=	ENSP00000415036.2:p.Gly385=
ENST00000497544.3:n.745G=
ENST00000636397.1:c.1037G=	ENSP00000489910.1:p.Gly346=
ENST00000636571.1:c.1016G=	ENSP00000490770.1:p.Gly339=
ENST00000636579.1:c.38G=	ENSP00000490489.1:p.Gly13=
ENST00000636615.1:c.1037G=	ENSP00000490014.1:p.Gly346=
ENST00000636843.1:c.1031G=	ENSP00000490897.1:p.Gly344=
ENST00000637158.1:n.635G=
ENST00000637381.2:n.3465G=
ENST00000637387.1:c.1016G=	ENSP00000490598.1:p.Gly339=
ENST00000637815.2:c.1019G=	ENSP00000490344.1:p.Gly340=
ENST00000637915.1:c.1037G=	ENSP00000490471.1:p.Gly346=
ENST00000637937.1:n.345G=
ENST00000678991.1:c.*898G=	ENSP00000503019.1:n.*898G=
ENST00000236671.6:c.1037G=	ENSP00000236671.2:p.Gly346=
ENST00000427721.2:c.437G=	ENSP00000415840.2:p.Gly146=
ENST00000429746.1:c.368G=	ENSP00000402586.1:p.Gly123=
ENST00000433655.5:c.*203G=	ENSP00000404902.1:n.*203G=
ENST00000497544.1:n.745G=
NM_001909.4:c.1037G=	NP_001900.1:p.Gly346=
NM_001909.5:c.1037G= MANE Select	NP_001900.1:p.Gly346=