Canonical Allele Identifier: CA379092535

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774824C>T (hg19) ; chr11:g.1753594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753594C>T , CM000673.2:g.1753594C>T	GRCh38
NC_000011.9:g.1774824C>T , CM000673.1:g.1774824C>T	GRCh37
NC_000011.8:g.1731400C>T	NCBI36
NG_008655.1:g.15399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1148G>A MANE Select	ENSP00000236671.2:p.Trp383Ter
ENST00000367196.4:c.1043G>A	ENSP00000356164.4:p.Trp348Ter
ENST00000427721.3:c.573G>A
ENST00000429746.2:c.1043G>A	ENSP00000402586.2:p.Trp348Ter
ENST00000433655.6:c.*314G>A	ENSP00000404902.1:n.*314G>A
ENST00000438213.6:c.1265G>A	ENSP00000415036.2:p.Trp422Ter
ENST00000636397.1:c.1071+209G>A	ENSP00000489910.1:n.1071+209G>A
ENST00000636571.1:c.1127G>A	ENSP00000490770.1:p.Trp376Ter
ENST00000636579.1:c.72+209G>A	ENSP00000490489.1:n.72+209G>A
ENST00000636615.1:c.1071+209G>A	ENSP00000490014.1:n.1071+209G>A
ENST00000636843.1:c.1142G>A	ENSP00000490897.1:p.Trp381Ter
ENST00000637158.1:n.746G>A
ENST00000637381.2:n.3576G>A
ENST00000637387.1:c.1127G>A	ENSP00000490598.1:p.Trp376Ter
ENST00000637815.2:c.1130G>A	ENSP00000490344.1:p.Trp377Ter
ENST00000637915.1:c.1139G>A	ENSP00000490471.1:p.Trp380Ter
ENST00000637937.1:n.456G>A
ENST00000678991.1:c.*1009G>A	ENSP00000503019.1:n.*1009G>A
ENST00000236671.6:c.1148G>A	ENSP00000236671.2:p.Trp383Ter
ENST00000427721.2:c.471+209G>A	ENSP00000415840.2:n.471+209G>A
ENST00000429746.1:c.479G>A	ENSP00000402586.1:p.Trp160Ter
ENST00000433655.5:c.*314G>A	ENSP00000404902.1:n.*314G>A
NM_001909.4:c.1148G>A	NP_001900.1:p.Trp383Ter
NM_001909.5:c.1148G>A MANE Select	NP_001900.1:p.Trp383Ter