Canonical Allele Identifier: CA471988713

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780855C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759625C>T , CM000673.2:g.1759625C>T	GRCh38
NC_000011.9:g.1780855C>T , CM000673.1:g.1780855C>T	GRCh37
NC_000011.8:g.1737431C>T	NCBI36
NG_008655.1:g.9368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.243G>A MANE Select	ENSP00000236671.2:p.Gly81=
ENST00000367196.4:c.138G>A	ENSP00000356164.4:p.Gly46=
ENST00000429746.2:c.138G>A	ENSP00000402586.2:p.Gly46=
ENST00000433655.6:c.243G>A	ENSP00000404902.1:p.Gly81=
ENST00000438213.6:c.243G>A	ENSP00000415036.2:p.Gly81=
ENST00000636397.1:c.243G>A	ENSP00000489910.1:p.Gly81=
ENST00000636571.1:c.222G>A	ENSP00000490770.1:p.Gly74=
ENST00000636615.1:c.243G>A	ENSP00000490014.1:p.Gly81=
ENST00000636843.1:c.237G>A	ENSP00000490897.1:p.Gly79=
ENST00000637381.2:n.2671G>A
ENST00000637387.1:c.243G>A	ENSP00000490598.1:p.Gly81=
ENST00000637815.2:c.243G>A	ENSP00000490344.1:p.Gly81=
ENST00000637915.1:c.243G>A	ENSP00000490471.1:p.Gly81=
ENST00000677300.1:n.638G>A
ENST00000678991.1:c.*104G>A	ENSP00000503019.1:n.*104G>A
ENST00000236671.6:c.243G>A	ENSP00000236671.2:p.Gly81=
ENST00000367196.3:c.138G>A	ENSP00000356164.3:p.Gly46=
ENST00000433655.5:c.243G>A	ENSP00000404902.1:p.Gly81=
ENST00000438213.5:c.198G>A	ENSP00000415036.1:p.Gly66=
NM_001909.4:c.243G>A	NP_001900.1:p.Gly81=
NM_001909.5:c.243G>A MANE Select	NP_001900.1:p.Gly81=