Canonical Allele Identifier: CA379092865

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1775046T>A (hg19) ; chr11:g.1753816T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753816T>A , CM000673.2:g.1753816T>A	GRCh38
NC_000011.9:g.1775046T>A , CM000673.1:g.1775046T>A	GRCh37
NC_000011.8:g.1731622T>A	NCBI36
NG_008655.1:g.15177A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1058A>T MANE Select	ENSP00000236671.2:p.Asp353Val
ENST00000367196.4:c.953A>T	ENSP00000356164.4:p.Asp318Val
ENST00000427721.3:c.483A>T
ENST00000429746.2:c.953A>T	ENSP00000402586.2:p.Asp318Val
ENST00000433655.6:c.*224A>T	ENSP00000404902.1:n.*224A>T
ENST00000438213.6:c.1175A>T	ENSP00000415036.2:p.Asp392Val
ENST00000497544.3:n.766A>T
ENST00000636397.1:c.1058A>T	ENSP00000489910.1:p.Asp353Val
ENST00000636571.1:c.1037A>T	ENSP00000490770.1:p.Asp346Val
ENST00000636579.1:c.59A>T	ENSP00000490489.1:p.Asp20Val
ENST00000636615.1:c.1058A>T	ENSP00000490014.1:p.Asp353Val
ENST00000636843.1:c.1052A>T	ENSP00000490897.1:p.Asp351Val
ENST00000637158.1:n.656A>T
ENST00000637381.2:n.3486A>T
ENST00000637387.1:c.1037A>T	ENSP00000490598.1:p.Asp346Val
ENST00000637815.2:c.1040A>T	ENSP00000490344.1:p.Asp347Val
ENST00000637915.1:c.1058A>T	ENSP00000490471.1:p.Asp353Val
ENST00000637937.1:n.366A>T
ENST00000678991.1:c.*919A>T	ENSP00000503019.1:n.*919A>T
ENST00000236671.6:c.1058A>T	ENSP00000236671.2:p.Asp353Val
ENST00000427721.2:c.458A>T	ENSP00000415840.2:p.Asp153Val
ENST00000429746.1:c.389A>T	ENSP00000402586.1:p.Asp130Val
ENST00000433655.5:c.*224A>T	ENSP00000404902.1:n.*224A>T
ENST00000497544.1:n.766A>T
NM_001909.4:c.1058A>T	NP_001900.1:p.Asp353Val
NM_001909.5:c.1058A>T MANE Select	NP_001900.1:p.Asp353Val