Canonical Allele Identifier: CA379098527

Gene: CTSD

Linked Data

• dbSNP Id: rs1554962843
• MyVariant Identifiers: chr11:g.1780847C>A (hg19) ; chr11:g.1759617C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759617C>A , CM000673.2:g.1759617C>A	GRCh38
NC_000011.9:g.1780847C>A , CM000673.1:g.1780847C>A	GRCh37
NC_000011.8:g.1737423C>A	NCBI36
NG_008655.1:g.9376G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.251G>T MANE Select	ENSP00000236671.2:p.Gly84Val
ENST00000367196.4:c.146G>T	ENSP00000356164.4:p.Gly49Val
ENST00000429746.2:c.146G>T	ENSP00000402586.2:p.Gly49Val
ENST00000433655.6:c.251G>T	ENSP00000404902.1:p.Gly84Val
ENST00000438213.6:c.251G>T	ENSP00000415036.2:p.Gly84Val
ENST00000636397.1:c.251G>T	ENSP00000489910.1:p.Gly84Val
ENST00000636571.1:c.230G>T	ENSP00000490770.1:p.Gly77Val
ENST00000636615.1:c.251G>T	ENSP00000490014.1:p.Gly84Val
ENST00000636843.1:c.245G>T	ENSP00000490897.1:p.Gly82Val
ENST00000637381.2:n.2679G>T
ENST00000637387.1:c.251G>T	ENSP00000490598.1:p.Gly84Val
ENST00000637815.2:c.251G>T	ENSP00000490344.1:p.Gly84Val
ENST00000637915.1:c.251G>T	ENSP00000490471.1:p.Gly84Val
ENST00000677300.1:n.646G>T
ENST00000678991.1:c.*112G>T	ENSP00000503019.1:n.*112G>T
ENST00000236671.6:c.251G>T	ENSP00000236671.2:p.Gly84Val
ENST00000367196.3:c.146G>T	ENSP00000356164.3:p.Gly49Val
ENST00000433655.5:c.251G>T	ENSP00000404902.1:p.Gly84Val
ENST00000438213.5:c.206G>T	ENSP00000415036.1:p.Gly69Val
NM_001909.4:c.251G>T	NP_001900.1:p.Gly84Val
NM_001909.5:c.251G>T MANE Select	NP_001900.1:p.Gly84Val