Canonical Allele Identifier: CA1947825373

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753997G= , CM000673.2:g.1753997G=	GRCh38
NC_000011.9:g.1775227G= , CM000673.1:g.1775227G=	GRCh37
NC_000011.8:g.1731803G=	NCBI36
NG_008655.1:g.14996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.969C= MANE Select	ENSP00000236671.2:p.Gly323=
ENST00000367196.4:c.864C=	ENSP00000356164.4:p.Gly288=
ENST00000427721.3:c.394C=
ENST00000429746.2:c.864C=	ENSP00000402586.2:p.Gly288=
ENST00000433655.6:c.*135C=	ENSP00000404902.1:n.*135C=
ENST00000438213.6:c.1086C=	ENSP00000415036.2:p.Gly362=
ENST00000497544.3:n.585C=
ENST00000636397.1:c.969C=	ENSP00000489910.1:p.Gly323=
ENST00000636571.1:c.948C=	ENSP00000490770.1:p.Gly316=
ENST00000636615.1:c.969C=	ENSP00000490014.1:p.Gly323=
ENST00000636843.1:c.963C=	ENSP00000490897.1:p.Gly321=
ENST00000637158.1:n.567C=
ENST00000637381.2:n.3397C=
ENST00000637387.1:c.969C=	ENSP00000490598.1:p.Gly323=
ENST00000637815.2:c.951C=	ENSP00000490344.1:p.Gly317=
ENST00000637915.1:c.969C=	ENSP00000490471.1:p.Gly323=
ENST00000637937.1:n.277C=
ENST00000678991.1:c.*830C=	ENSP00000503019.1:n.*830C=
ENST00000236671.6:c.969C=	ENSP00000236671.2:p.Gly323=
ENST00000427721.2:c.369C=	ENSP00000415840.2:p.Gly123=
ENST00000429746.1:c.300C=	ENSP00000402586.1:p.Gly100=
ENST00000433655.5:c.*135C=	ENSP00000404902.1:n.*135C=
ENST00000497544.1:n.585C=
NM_001909.4:c.969C=	NP_001900.1:p.Gly323=
NM_001909.5:c.969C= MANE Select	NP_001900.1:p.Gly323=