Canonical Allele Identifier: CA379099552

Gene: CTSD

Linked Data

• COSMIC: COSM5562731
• MyVariant Identifiers: chr11:g.1782589G>T (hg19) ; chr11:g.1761359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1761359G>T , CM000673.2:g.1761359G>T	GRCh38
NC_000011.9:g.1782589G>T , CM000673.1:g.1782589G>T	GRCh37
NC_000011.8:g.1739165G>T	NCBI36
NG_008655.1:g.7634C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.178C>A MANE Select	ENSP00000236671.2:p.Pro60Thr
ENST00000367196.4:c.73C>A	ENSP00000356164.4:p.Pro25Thr
ENST00000429746.2:c.73C>A	ENSP00000402586.2:p.Pro25Thr
ENST00000433655.6:c.178C>A	ENSP00000404902.1:p.Pro60Thr
ENST00000438213.6:c.178C>A	ENSP00000415036.2:p.Pro60Thr
ENST00000636397.1:c.178C>A	ENSP00000489910.1:p.Pro60Thr
ENST00000636571.1:c.178C>A	ENSP00000490770.1:p.Pro60Thr
ENST00000636615.1:c.178C>A	ENSP00000490014.1:p.Pro60Thr
ENST00000636843.1:c.178C>A	ENSP00000490897.1:p.Pro60Thr
ENST00000637381.2:n.2606C>A
ENST00000637387.1:c.178C>A	ENSP00000490598.1:p.Pro60Thr
ENST00000637815.2:c.178C>A	ENSP00000490344.1:p.Pro60Thr
ENST00000637915.1:c.178C>A	ENSP00000490471.1:p.Pro60Thr
ENST00000678991.1:c.*39C>A	ENSP00000503019.1:n.*39C>A
ENST00000236671.6:c.178C>A	ENSP00000236671.2:p.Pro60Thr
ENST00000367196.3:c.73C>A	ENSP00000356164.3:p.Pro25Thr
ENST00000433655.5:c.178C>A	ENSP00000404902.1:p.Pro60Thr
ENST00000438213.5:c.133C>A	ENSP00000415036.1:p.Pro45Thr
NM_001909.4:c.178C>A	NP_001900.1:p.Pro60Thr
NM_001909.5:c.178C>A MANE Select	NP_001900.1:p.Pro60Thr