Canonical Allele Identifier: CA1947825383

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754017C= , CM000673.2:g.1754017C=	GRCh38
NC_000011.9:g.1775247C= , CM000673.1:g.1775247C=	GRCh37
NC_000011.8:g.1731823C=	NCBI36
NG_008655.1:g.14976G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.949G= MANE Select	ENSP00000236671.2:p.Ala317=
ENST00000367196.4:c.844G=	ENSP00000356164.4:p.Ala282=
ENST00000427721.3:c.374G=
ENST00000429746.2:c.844G=	ENSP00000402586.2:p.Ala282=
ENST00000433655.6:c.*115G=	ENSP00000404902.1:n.*115G=
ENST00000438213.6:c.1066G=	ENSP00000415036.2:p.Ala356=
ENST00000497544.3:n.565G=
ENST00000636397.1:c.949G=	ENSP00000489910.1:p.Ala317=
ENST00000636571.1:c.928G=	ENSP00000490770.1:p.Ala310=
ENST00000636615.1:c.949G=	ENSP00000490014.1:p.Ala317=
ENST00000636843.1:c.943G=	ENSP00000490897.1:p.Ala315=
ENST00000637158.1:n.547G=
ENST00000637381.2:n.3377G=
ENST00000637387.1:c.949G=	ENSP00000490598.1:p.Ala317=
ENST00000637815.2:c.931G=	ENSP00000490344.1:p.Ala311=
ENST00000637915.1:c.949G=	ENSP00000490471.1:p.Ala317=
ENST00000637937.1:n.257G=
ENST00000678991.1:c.*810G=	ENSP00000503019.1:n.*810G=
ENST00000236671.6:c.949G=	ENSP00000236671.2:p.Ala317=
ENST00000427721.2:c.349G=	ENSP00000415840.2:p.Ala117=
ENST00000429746.1:c.280G=	ENSP00000402586.1:p.Ala94=
ENST00000433655.5:c.*115G=	ENSP00000404902.1:n.*115G=
ENST00000497544.1:n.565G=
NM_001909.4:c.949G=	NP_001900.1:p.Ala317=
NM_001909.5:c.949G= MANE Select	NP_001900.1:p.Ala317=