Canonical Allele Identifier: CA1947825283

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753847C= , CM000673.2:g.1753847C=	GRCh38
NC_000011.9:g.1775077C= , CM000673.1:g.1775077C=	GRCh37
NC_000011.8:g.1731653C=	NCBI36
NG_008655.1:g.15146G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1027G= MANE Select	ENSP00000236671.2:p.Gly343=
ENST00000367196.4:c.922G=	ENSP00000356164.4:p.Gly308=
ENST00000427721.3:c.452G=
ENST00000429746.2:c.922G=	ENSP00000402586.2:p.Gly308=
ENST00000433655.6:c.*193G=	ENSP00000404902.1:n.*193G=
ENST00000438213.6:c.1144G=	ENSP00000415036.2:p.Gly382=
ENST00000497544.3:n.735G=
ENST00000636397.1:c.1027G=	ENSP00000489910.1:p.Gly343=
ENST00000636571.1:c.1006G=	ENSP00000490770.1:p.Gly336=
ENST00000636579.1:c.28G=	ENSP00000490489.1:p.Gly10=
ENST00000636615.1:c.1027G=	ENSP00000490014.1:p.Gly343=
ENST00000636843.1:c.1021G=	ENSP00000490897.1:p.Gly341=
ENST00000637158.1:n.625G=
ENST00000637381.2:n.3455G=
ENST00000637387.1:c.1006G=	ENSP00000490598.1:p.Gly336=
ENST00000637815.2:c.1009G=	ENSP00000490344.1:p.Gly337=
ENST00000637915.1:c.1027G=	ENSP00000490471.1:p.Gly343=
ENST00000637937.1:n.335G=
ENST00000678991.1:c.*888G=	ENSP00000503019.1:n.*888G=
ENST00000236671.6:c.1027G=	ENSP00000236671.2:p.Gly343=
ENST00000427721.2:c.427G=	ENSP00000415840.2:p.Gly143=
ENST00000429746.1:c.358G=	ENSP00000402586.1:p.Gly120=
ENST00000433655.5:c.*193G=	ENSP00000404902.1:n.*193G=
ENST00000497544.1:n.735G=
NM_001909.4:c.1027G=	NP_001900.1:p.Gly343=
NM_001909.5:c.1027G= MANE Select	NP_001900.1:p.Gly343=