Canonical Allele Identifier: CA1947828430

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1758994C= , CM000673.2:g.1758994C=	GRCh38
NC_000011.9:g.1780224C= , CM000673.1:g.1780224C=	GRCh37
NC_000011.8:g.1736800C=	NCBI36
NG_008655.1:g.9999G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001909.5:c.446G= MANE Select	NP_001900.1:p.Gly149=
ENST00000236671.7:c.446G= MANE Select	ENSP00000236671.2:p.Gly149=
NM_001909.4:c.446G=	NP_001900.1:p.Gly149=
ENST00000236671.6:c.446G=	ENSP00000236671.2:p.Gly149=
ENST00000367196.3:c.341G=	ENSP00000356164.3:p.Gly114=
ENST00000367196.4:c.341G=	ENSP00000356164.4:p.Gly114=
ENST00000427721.2:c.-155G=	ENSP00000415840.2:n.-155G=
ENST00000429746.2:c.341G=	ENSP00000402586.2:p.Gly114=
ENST00000433655.5:c.446G=	ENSP00000404902.1:p.Gly149=
ENST00000433655.6:c.446G=	ENSP00000404902.1:p.Gly149=
ENST00000438213.5:c.401G=	ENSP00000415036.1:p.Gly134=
ENST00000438213.6:c.446G=	ENSP00000415036.2:p.Gly149=
ENST00000636397.1:c.446G=	ENSP00000489910.1:p.Gly149=
ENST00000636571.1:c.425G=	ENSP00000490770.1:p.Gly142=
ENST00000636615.1:c.446G=	ENSP00000490014.1:p.Gly149=
ENST00000636843.1:c.440G=	ENSP00000490897.1:p.Gly147=
ENST00000637381.2:n.2874G=
ENST00000637387.1:c.446G=	ENSP00000490598.1:p.Gly149=
ENST00000637815.2:c.446G=	ENSP00000490344.1:p.Gly149=
ENST00000637915.1:c.446G=	ENSP00000490471.1:p.Gly149=
ENST00000677300.1:n.841G=
ENST00000678991.1:c.*307G=	ENSP00000503019.1:n.*307G=