Canonical Allele Identifier: CA379092359

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774763C>A (hg19) ; chr11:g.1753533C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753533C>A , CM000673.2:g.1753533C>A	GRCh38
NC_000011.9:g.1774763C>A , CM000673.1:g.1774763C>A	GRCh37
NC_000011.8:g.1731339C>A	NCBI36
NG_008655.1:g.15460G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1209G>T MANE Select	ENSP00000236671.2:p.Arg403Ser
ENST00000367196.4:c.1104G>T	ENSP00000356164.4:p.Arg368Ser
ENST00000427721.3:c.634G>T
ENST00000429746.2:c.1104G>T	ENSP00000402586.2:p.Arg368Ser
ENST00000433655.6:c.*375G>T	ENSP00000404902.1:n.*375G>T
ENST00000438213.6:c.1326G>T	ENSP00000415036.2:p.Arg442Ser
ENST00000636397.1:c.1071+270G>T	ENSP00000489910.1:n.1071+270G>T
ENST00000636571.1:c.1188G>T	ENSP00000490770.1:p.Arg396Ser
ENST00000636579.1:c.72+270G>T	ENSP00000490489.1:n.72+270G>T
ENST00000636615.1:c.1071+270G>T	ENSP00000490014.1:n.1071+270G>T
ENST00000636843.1:c.1203G>T	ENSP00000490897.1:p.Arg401Ser
ENST00000637158.1:n.807G>T
ENST00000637381.2:n.3637G>T
ENST00000637387.1:c.1188G>T	ENSP00000490598.1:p.Arg396Ser
ENST00000637815.2:c.1191G>T	ENSP00000490344.1:p.Arg397Ser
ENST00000637915.1:c.1200G>T	ENSP00000490471.1:p.Arg400Ser
ENST00000637937.1:n.517G>T
ENST00000678991.1:c.*1070G>T	ENSP00000503019.1:n.*1070G>T
ENST00000236671.6:c.1209G>T	ENSP00000236671.2:p.Arg403Ser
ENST00000427721.2:c.471+270G>T	ENSP00000415840.2:n.471+270G>T
ENST00000429746.1:c.540G>T	ENSP00000402586.1:p.Arg180Ser
ENST00000433655.5:c.*375G>T	ENSP00000404902.1:n.*375G>T
NM_001909.4:c.1209G>T	NP_001900.1:p.Arg403Ser
NM_001909.5:c.1209G>T MANE Select	NP_001900.1:p.Arg403Ser