Canonical Allele Identifier: CA1947825290

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753864G= , CM000673.2:g.1753864G=	GRCh38
NC_000011.9:g.1775094G= , CM000673.1:g.1775094G=	GRCh37
NC_000011.8:g.1731670G=	NCBI36
NG_008655.1:g.15129C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1010C= MANE Select	ENSP00000236671.2:p.Ala337=
ENST00000367196.4:c.905C=	ENSP00000356164.4:p.Ala302=
ENST00000427721.3:c.435C=
ENST00000429746.2:c.905C=	ENSP00000402586.2:p.Ala302=
ENST00000433655.6:c.*176C=	ENSP00000404902.1:n.*176C=
ENST00000438213.6:c.1127C=	ENSP00000415036.2:p.Ala376=
ENST00000497544.3:n.718C=
ENST00000636397.1:c.1010C=	ENSP00000489910.1:p.Ala337=
ENST00000636571.1:c.989C=	ENSP00000490770.1:p.Ala330=
ENST00000636579.1:c.11C=	ENSP00000490489.1:p.Ala4=
ENST00000636615.1:c.1010C=	ENSP00000490014.1:p.Ala337=
ENST00000636843.1:c.1004C=	ENSP00000490897.1:p.Ala335=
ENST00000637158.1:n.608C=
ENST00000637381.2:n.3438C=
ENST00000637387.1:c.989C=	ENSP00000490598.1:p.Ala330=
ENST00000637815.2:c.992C=	ENSP00000490344.1:p.Ala331=
ENST00000637915.1:c.1010C=	ENSP00000490471.1:p.Ala337=
ENST00000637937.1:n.318C=
ENST00000678991.1:c.*871C=	ENSP00000503019.1:n.*871C=
ENST00000236671.6:c.1010C=	ENSP00000236671.2:p.Ala337=
ENST00000427721.2:c.410C=	ENSP00000415840.2:p.Ala137=
ENST00000429746.1:c.341C=	ENSP00000402586.1:p.Ala114=
ENST00000433655.5:c.*176C=	ENSP00000404902.1:n.*176C=
ENST00000497544.1:n.718C=
NM_001909.4:c.1010C=	NP_001900.1:p.Ala337=
NM_001909.5:c.1010C= MANE Select	NP_001900.1:p.Ala337=