Canonical Allele Identifier: CA379093484

Gene: CTSD

Linked Data

• dbSNP Id: rs1228893772
• gnomAD v3: 11-1753995-T-A
• gnomAD v4: 11-1753995-T-A
• MyVariant Identifiers: chr11:g.1775225T>A (hg19) ; chr11:g.1753995T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753995T>A , CM000673.2:g.1753995T>A	GRCh38
NC_000011.9:g.1775225T>A , CM000673.1:g.1775225T>A	GRCh37
NC_000011.8:g.1731801T>A	NCBI36
NG_008655.1:g.14998A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.971A>T MANE Select	ENSP00000236671.2:p.Glu324Val
ENST00000367196.4:c.866A>T	ENSP00000356164.4:p.Glu289Val
ENST00000427721.3:c.396A>T
ENST00000429746.2:c.866A>T	ENSP00000402586.2:p.Glu289Val
ENST00000433655.6:c.*137A>T	ENSP00000404902.1:n.*137A>T
ENST00000438213.6:c.1088A>T	ENSP00000415036.2:p.Glu363Val
ENST00000497544.3:n.587A>T
ENST00000636397.1:c.971A>T	ENSP00000489910.1:p.Glu324Val
ENST00000636571.1:c.950A>T	ENSP00000490770.1:p.Glu317Val
ENST00000636615.1:c.971A>T	ENSP00000490014.1:p.Glu324Val
ENST00000636843.1:c.965A>T	ENSP00000490897.1:p.Glu322Val
ENST00000637158.1:n.569A>T
ENST00000637381.2:n.3399A>T
ENST00000637387.1:c.971A>T	ENSP00000490598.1:p.Glu324Val
ENST00000637815.2:c.953A>T	ENSP00000490344.1:p.Glu318Val
ENST00000637915.1:c.971A>T	ENSP00000490471.1:p.Glu324Val
ENST00000637937.1:n.279A>T
ENST00000678991.1:c.*832A>T	ENSP00000503019.1:n.*832A>T
ENST00000236671.6:c.971A>T	ENSP00000236671.2:p.Glu324Val
ENST00000427721.2:c.371A>T	ENSP00000415840.2:p.Glu124Val
ENST00000429746.1:c.302A>T	ENSP00000402586.1:p.Glu101Val
ENST00000433655.5:c.*137A>T	ENSP00000404902.1:n.*137A>T
ENST00000497544.1:n.587A>T
NM_001909.4:c.971A>T	NP_001900.1:p.Glu324Val
NM_001909.5:c.971A>T MANE Select	NP_001900.1:p.Glu324Val