Canonical Allele Identifier: CA471988517

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780819T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759589T>C , CM000673.2:g.1759589T>C	GRCh38
NC_000011.9:g.1780819T>C , CM000673.1:g.1780819T>C	GRCh37
NC_000011.8:g.1737395T>C	NCBI36
NG_008655.1:g.9404A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.279A>G MANE Select	ENSP00000236671.2:p.Thr93=
ENST00000367196.4:c.174A>G	ENSP00000356164.4:p.Thr58=
ENST00000429746.2:c.174A>G	ENSP00000402586.2:p.Thr58=
ENST00000433655.6:c.279A>G	ENSP00000404902.1:p.Thr93=
ENST00000438213.6:c.279A>G	ENSP00000415036.2:p.Thr93=
ENST00000636397.1:c.279A>G	ENSP00000489910.1:p.Thr93=
ENST00000636571.1:c.258A>G	ENSP00000490770.1:p.Thr86=
ENST00000636615.1:c.279A>G	ENSP00000490014.1:p.Thr93=
ENST00000636843.1:c.273A>G	ENSP00000490897.1:p.Thr91=
ENST00000637381.2:n.2707A>G
ENST00000637387.1:c.279A>G	ENSP00000490598.1:p.Thr93=
ENST00000637815.2:c.279A>G	ENSP00000490344.1:p.Thr93=
ENST00000637915.1:c.279A>G	ENSP00000490471.1:p.Thr93=
ENST00000677300.1:n.674A>G
ENST00000678991.1:c.*140A>G	ENSP00000503019.1:n.*140A>G
ENST00000236671.6:c.279A>G	ENSP00000236671.2:p.Thr93=
ENST00000367196.3:c.174A>G	ENSP00000356164.3:p.Thr58=
ENST00000433655.5:c.279A>G	ENSP00000404902.1:p.Thr93=
ENST00000438213.5:c.234A>G	ENSP00000415036.1:p.Thr78=
NM_001909.4:c.279A>G	NP_001900.1:p.Thr93=
NM_001909.5:c.279A>G MANE Select	NP_001900.1:p.Thr93=