Canonical Allele Identifier: CA379092631

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774850G>T (hg19) ; chr11:g.1753620G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753620G>T , CM000673.2:g.1753620G>T	GRCh38
NC_000011.9:g.1774850G>T , CM000673.1:g.1774850G>T	GRCh37
NC_000011.8:g.1731426G>T	NCBI36
NG_008655.1:g.15373C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1122C>A MANE Select	ENSP00000236671.2:p.Asp374Glu
ENST00000367196.4:c.1017C>A	ENSP00000356164.4:p.Asp339Glu
ENST00000427721.3:c.547C>A
ENST00000429746.2:c.1017C>A	ENSP00000402586.2:p.Asp339Glu
ENST00000433655.6:c.*288C>A	ENSP00000404902.1:n.*288C>A
ENST00000438213.6:c.1239C>A	ENSP00000415036.2:p.Asp413Glu
ENST00000636397.1:c.1071+183C>A	ENSP00000489910.1:n.1071+183C>A
ENST00000636571.1:c.1101C>A	ENSP00000490770.1:p.Asp367Glu
ENST00000636579.1:c.72+183C>A	ENSP00000490489.1:n.72+183C>A
ENST00000636615.1:c.1071+183C>A	ENSP00000490014.1:n.1071+183C>A
ENST00000636843.1:c.1116C>A	ENSP00000490897.1:p.Asp372Glu
ENST00000637158.1:n.720C>A
ENST00000637381.2:n.3550C>A
ENST00000637387.1:c.1101C>A	ENSP00000490598.1:p.Asp367Glu
ENST00000637815.2:c.1104C>A	ENSP00000490344.1:p.Asp368Glu
ENST00000637915.1:c.1113C>A	ENSP00000490471.1:p.Asp371Glu
ENST00000637937.1:n.430C>A
ENST00000678991.1:c.*983C>A	ENSP00000503019.1:n.*983C>A
ENST00000236671.6:c.1122C>A	ENSP00000236671.2:p.Asp374Glu
ENST00000427721.2:c.471+183C>A	ENSP00000415840.2:n.471+183C>A
ENST00000429746.1:c.453C>A	ENSP00000402586.1:p.Asp151Glu
ENST00000433655.5:c.*288C>A	ENSP00000404902.1:n.*288C>A
NM_001909.4:c.1122C>A	NP_001900.1:p.Asp374Glu
NM_001909.5:c.1122C>A MANE Select	NP_001900.1:p.Asp374Glu