Canonical Allele Identifier: CA1947825398

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754041G= , CM000673.2:g.1754041G=	GRCh38
NC_000011.9:g.1775271G= , CM000673.1:g.1775271G=	GRCh37
NC_000011.8:g.1731847G=	NCBI36
NG_008655.1:g.14952C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.925C= MANE Select	ENSP00000236671.2:p.Arg309=
ENST00000367196.4:c.820C=	ENSP00000356164.4:p.Arg274=
ENST00000427721.3:c.350C=
ENST00000429746.2:c.820C=	ENSP00000402586.2:p.Arg274=
ENST00000433655.6:c.*91C=	ENSP00000404902.1:n.*91C=
ENST00000438213.6:c.1042C=	ENSP00000415036.2:p.Arg348=
ENST00000497544.3:n.541C=
ENST00000636397.1:c.925C=	ENSP00000489910.1:p.Arg309=
ENST00000636571.1:c.904C=	ENSP00000490770.1:p.Arg302=
ENST00000636615.1:c.925C=	ENSP00000490014.1:p.Arg309=
ENST00000636843.1:c.919C=	ENSP00000490897.1:p.Arg307=
ENST00000637158.1:n.523C=
ENST00000637381.2:n.3353C=
ENST00000637387.1:c.925C=	ENSP00000490598.1:p.Arg309=
ENST00000637815.2:c.907C=	ENSP00000490344.1:p.Arg303=
ENST00000637915.1:c.925C=	ENSP00000490471.1:p.Arg309=
ENST00000637937.1:n.233C=
ENST00000678991.1:c.*786C=	ENSP00000503019.1:n.*786C=
ENST00000236671.6:c.925C=	ENSP00000236671.2:p.Arg309=
ENST00000427721.2:c.325C=	ENSP00000415840.2:p.Arg109=
ENST00000429746.1:c.256C=	ENSP00000402586.1:p.Arg86=
ENST00000433655.5:c.*91C=	ENSP00000404902.1:n.*91C=
ENST00000438213.5:c.880C=	ENSP00000415036.1:p.Arg294=
ENST00000497544.1:n.541C=
NM_001909.4:c.925C=	NP_001900.1:p.Arg309=
NM_001909.5:c.925C= MANE Select	NP_001900.1:p.Arg309=