Canonical Allele Identifier: CA379092641

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774852C>A (hg19) ; chr11:g.1753622C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753622C>A , CM000673.2:g.1753622C>A	GRCh38
NC_000011.9:g.1774852C>A , CM000673.1:g.1774852C>A	GRCh37
NC_000011.8:g.1731428C>A	NCBI36
NG_008655.1:g.15371G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1120G>T MANE Select	ENSP00000236671.2:p.Asp374Tyr
ENST00000367196.4:c.1015G>T	ENSP00000356164.4:p.Asp339Tyr
ENST00000427721.3:c.545G>T
ENST00000429746.2:c.1015G>T	ENSP00000402586.2:p.Asp339Tyr
ENST00000433655.6:c.*286G>T	ENSP00000404902.1:n.*286G>T
ENST00000438213.6:c.1237G>T	ENSP00000415036.2:p.Asp413Tyr
ENST00000636397.1:c.1071+181G>T	ENSP00000489910.1:n.1071+181G>T
ENST00000636571.1:c.1099G>T	ENSP00000490770.1:p.Asp367Tyr
ENST00000636579.1:c.72+181G>T	ENSP00000490489.1:n.72+181G>T
ENST00000636615.1:c.1071+181G>T	ENSP00000490014.1:n.1071+181G>T
ENST00000636843.1:c.1114G>T	ENSP00000490897.1:p.Asp372Tyr
ENST00000637158.1:n.718G>T
ENST00000637381.2:n.3548G>T
ENST00000637387.1:c.1099G>T	ENSP00000490598.1:p.Asp367Tyr
ENST00000637815.2:c.1102G>T	ENSP00000490344.1:p.Asp368Tyr
ENST00000637915.1:c.1111G>T	ENSP00000490471.1:p.Asp371Tyr
ENST00000637937.1:n.428G>T
ENST00000678991.1:c.*981G>T	ENSP00000503019.1:n.*981G>T
ENST00000236671.6:c.1120G>T	ENSP00000236671.2:p.Asp374Tyr
ENST00000427721.2:c.471+181G>T	ENSP00000415840.2:n.471+181G>T
ENST00000429746.1:c.451G>T	ENSP00000402586.1:p.Asp151Tyr
ENST00000433655.5:c.*286G>T	ENSP00000404902.1:n.*286G>T
NM_001909.4:c.1120G>T	NP_001900.1:p.Asp374Tyr
NM_001909.5:c.1120G>T MANE Select	NP_001900.1:p.Asp374Tyr