Canonical Allele Identifier: CA379098444

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780827A>C (hg19) ; chr11:g.1759597A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759597A>C , CM000673.2:g.1759597A>C	GRCh38
NC_000011.9:g.1780827A>C , CM000673.1:g.1780827A>C	GRCh37
NC_000011.8:g.1737403A>C	NCBI36
NG_008655.1:g.9396T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.271T>G MANE Select	ENSP00000236671.2:p.Cys91Gly
ENST00000367196.4:c.166T>G	ENSP00000356164.4:p.Cys56Gly
ENST00000429746.2:c.166T>G	ENSP00000402586.2:p.Cys56Gly
ENST00000433655.6:c.271T>G	ENSP00000404902.1:p.Cys91Gly
ENST00000438213.6:c.271T>G	ENSP00000415036.2:p.Cys91Gly
ENST00000636397.1:c.271T>G	ENSP00000489910.1:p.Cys91Gly
ENST00000636571.1:c.250T>G	ENSP00000490770.1:p.Cys84Gly
ENST00000636615.1:c.271T>G	ENSP00000490014.1:p.Cys91Gly
ENST00000636843.1:c.265T>G	ENSP00000490897.1:p.Cys89Gly
ENST00000637381.2:n.2699T>G
ENST00000637387.1:c.271T>G	ENSP00000490598.1:p.Cys91Gly
ENST00000637815.2:c.271T>G	ENSP00000490344.1:p.Cys91Gly
ENST00000637915.1:c.271T>G	ENSP00000490471.1:p.Cys91Gly
ENST00000677300.1:n.666T>G
ENST00000678991.1:c.*132T>G	ENSP00000503019.1:n.*132T>G
ENST00000236671.6:c.271T>G	ENSP00000236671.2:p.Cys91Gly
ENST00000367196.3:c.166T>G	ENSP00000356164.3:p.Cys56Gly
ENST00000433655.5:c.271T>G	ENSP00000404902.1:p.Cys91Gly
ENST00000438213.5:c.226T>G	ENSP00000415036.1:p.Cys76Gly
NM_001909.4:c.271T>G	NP_001900.1:p.Cys91Gly
NM_001909.5:c.271T>G MANE Select	NP_001900.1:p.Cys91Gly