Canonical Allele Identifier: CA379092410

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774785A>C (hg19) ; chr11:g.1753555A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753555A>C , CM000673.2:g.1753555A>C	GRCh38
NC_000011.9:g.1774785A>C , CM000673.1:g.1774785A>C	GRCh37
NC_000011.8:g.1731361A>C	NCBI36
NG_008655.1:g.15438T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1187T>G MANE Select	ENSP00000236671.2:p.Val396Gly
ENST00000367196.4:c.1082T>G	ENSP00000356164.4:p.Val361Gly
ENST00000427721.3:c.612T>G
ENST00000429746.2:c.1082T>G	ENSP00000402586.2:p.Val361Gly
ENST00000433655.6:c.*353T>G	ENSP00000404902.1:n.*353T>G
ENST00000438213.6:c.1304T>G	ENSP00000415036.2:p.Val435Gly
ENST00000636397.1:c.1071+248T>G	ENSP00000489910.1:n.1071+248T>G
ENST00000636571.1:c.1166T>G	ENSP00000490770.1:p.Val389Gly
ENST00000636579.1:c.72+248T>G	ENSP00000490489.1:n.72+248T>G
ENST00000636615.1:c.1071+248T>G	ENSP00000490014.1:n.1071+248T>G
ENST00000636843.1:c.1181T>G	ENSP00000490897.1:p.Val394Gly
ENST00000637158.1:n.785T>G
ENST00000637381.2:n.3615T>G
ENST00000637387.1:c.1166T>G	ENSP00000490598.1:p.Val389Gly
ENST00000637815.2:c.1169T>G	ENSP00000490344.1:p.Val390Gly
ENST00000637915.1:c.1178T>G	ENSP00000490471.1:p.Val393Gly
ENST00000637937.1:n.495T>G
ENST00000678991.1:c.*1048T>G	ENSP00000503019.1:n.*1048T>G
ENST00000236671.6:c.1187T>G	ENSP00000236671.2:p.Val396Gly
ENST00000427721.2:c.471+248T>G	ENSP00000415840.2:n.471+248T>G
ENST00000429746.1:c.518T>G	ENSP00000402586.1:p.Val173Gly
ENST00000433655.5:c.*353T>G	ENSP00000404902.1:n.*353T>G
NM_001909.4:c.1187T>G	NP_001900.1:p.Val396Gly
NM_001909.5:c.1187T>G MANE Select	NP_001900.1:p.Val396Gly