Canonical Allele Identifier: CA379092678

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774863A>C (hg19) ; chr11:g.1753633A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753633A>C , CM000673.2:g.1753633A>C	GRCh38
NC_000011.9:g.1774863A>C , CM000673.1:g.1774863A>C	GRCh37
NC_000011.8:g.1731439A>C	NCBI36
NG_008655.1:g.15360T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1109T>G MANE Select	ENSP00000236671.2:p.Phe370Cys
ENST00000367196.4:c.1004T>G	ENSP00000356164.4:p.Phe335Cys
ENST00000427721.3:c.534T>G
ENST00000429746.2:c.1004T>G	ENSP00000402586.2:p.Phe335Cys
ENST00000433655.6:c.*275T>G	ENSP00000404902.1:n.*275T>G
ENST00000438213.6:c.1226T>G	ENSP00000415036.2:p.Phe409Cys
ENST00000636397.1:c.1071+170T>G	ENSP00000489910.1:n.1071+170T>G
ENST00000636571.1:c.1088T>G	ENSP00000490770.1:p.Phe363Cys
ENST00000636579.1:c.72+170T>G	ENSP00000490489.1:n.72+170T>G
ENST00000636615.1:c.1071+170T>G	ENSP00000490014.1:n.1071+170T>G
ENST00000636843.1:c.1103T>G	ENSP00000490897.1:p.Phe368Cys
ENST00000637158.1:n.707T>G
ENST00000637381.2:n.3537T>G
ENST00000637387.1:c.1088T>G	ENSP00000490598.1:p.Phe363Cys
ENST00000637815.2:c.1091T>G	ENSP00000490344.1:p.Phe364Cys
ENST00000637915.1:c.1100T>G	ENSP00000490471.1:p.Phe367Cys
ENST00000637937.1:n.417T>G
ENST00000678991.1:c.*970T>G	ENSP00000503019.1:n.*970T>G
ENST00000236671.6:c.1109T>G	ENSP00000236671.2:p.Phe370Cys
ENST00000427721.2:c.471+170T>G	ENSP00000415840.2:n.471+170T>G
ENST00000429746.1:c.440T>G	ENSP00000402586.1:p.Phe147Cys
ENST00000433655.5:c.*275T>G	ENSP00000404902.1:n.*275T>G
NM_001909.4:c.1109T>G	NP_001900.1:p.Phe370Cys
NM_001909.5:c.1109T>G MANE Select	NP_001900.1:p.Phe370Cys