Canonical Allele Identifier: CA379098054

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780761G>T (hg19) ; chr11:g.1759531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759531G>T , CM000673.2:g.1759531G>T	GRCh38
NC_000011.9:g.1780761G>T , CM000673.1:g.1780761G>T	GRCh37
NC_000011.8:g.1737337G>T	NCBI36
NG_008655.1:g.9462C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.337C>A MANE Select	ENSP00000236671.2:p.Leu113Met
ENST00000367196.4:c.232C>A	ENSP00000356164.4:p.Leu78Met
ENST00000429746.2:c.232C>A	ENSP00000402586.2:p.Leu78Met
ENST00000433655.6:c.337C>A	ENSP00000404902.1:p.Leu113Met
ENST00000438213.6:c.337C>A	ENSP00000415036.2:p.Leu113Met
ENST00000636397.1:c.337C>A	ENSP00000489910.1:p.Leu113Met
ENST00000636571.1:c.316C>A	ENSP00000490770.1:p.Leu106Met
ENST00000636615.1:c.337C>A	ENSP00000490014.1:p.Leu113Met
ENST00000636843.1:c.331C>A	ENSP00000490897.1:p.Leu111Met
ENST00000637381.2:n.2765C>A
ENST00000637387.1:c.337C>A	ENSP00000490598.1:p.Leu113Met
ENST00000637815.2:c.337C>A	ENSP00000490344.1:p.Leu113Met
ENST00000637915.1:c.337C>A	ENSP00000490471.1:p.Leu113Met
ENST00000677300.1:n.732C>A
ENST00000678991.1:c.*198C>A	ENSP00000503019.1:n.*198C>A
ENST00000236671.6:c.337C>A	ENSP00000236671.2:p.Leu113Met
ENST00000367196.3:c.232C>A	ENSP00000356164.3:p.Leu78Met
ENST00000433655.5:c.337C>A	ENSP00000404902.1:p.Leu113Met
ENST00000438213.5:c.292C>A	ENSP00000415036.1:p.Leu98Met
NM_001909.4:c.337C>A	NP_001900.1:p.Leu113Met
NM_001909.5:c.337C>A MANE Select	NP_001900.1:p.Leu113Met