Canonical Allele Identifier: CA1947825375

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754001T= , CM000673.2:g.1754001T=	GRCh38
NC_000011.9:g.1775231T= , CM000673.1:g.1775231T=	GRCh37
NC_000011.8:g.1731807T=	NCBI36
NG_008655.1:g.14992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.965A= MANE Select	ENSP00000236671.2:p.Gln322=
ENST00000367196.4:c.860A=	ENSP00000356164.4:p.Gln287=
ENST00000427721.3:c.390A=
ENST00000429746.2:c.860A=	ENSP00000402586.2:p.Gln287=
ENST00000433655.6:c.*131A=	ENSP00000404902.1:n.*131A=
ENST00000438213.6:c.1082A=	ENSP00000415036.2:p.Gln361=
ENST00000497544.3:n.581A=
ENST00000636397.1:c.965A=	ENSP00000489910.1:p.Gln322=
ENST00000636571.1:c.944A=	ENSP00000490770.1:p.Gln315=
ENST00000636615.1:c.965A=	ENSP00000490014.1:p.Gln322=
ENST00000636843.1:c.959A=	ENSP00000490897.1:p.Gln320=
ENST00000637158.1:n.563A=
ENST00000637381.2:n.3393A=
ENST00000637387.1:c.965A=	ENSP00000490598.1:p.Gln322=
ENST00000637815.2:c.947A=	ENSP00000490344.1:p.Gln316=
ENST00000637915.1:c.965A=	ENSP00000490471.1:p.Gln322=
ENST00000637937.1:n.273A=
ENST00000678991.1:c.*826A=	ENSP00000503019.1:n.*826A=
ENST00000236671.6:c.965A=	ENSP00000236671.2:p.Gln322=
ENST00000427721.2:c.365A=	ENSP00000415840.2:p.Gln122=
ENST00000429746.1:c.296A=	ENSP00000402586.1:p.Gln99=
ENST00000433655.5:c.*131A=	ENSP00000404902.1:n.*131A=
ENST00000497544.1:n.581A=
NM_001909.4:c.965A=	NP_001900.1:p.Gln322=
NM_001909.5:c.965A= MANE Select	NP_001900.1:p.Gln322=