Canonical Allele Identifier: CA379095334

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1776208G>T (hg19) ; chr11:g.1754978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754978G>T , CM000673.2:g.1754978G>T	GRCh38
NC_000011.9:g.1776208G>T , CM000673.1:g.1776208G>T	GRCh37
NC_000011.8:g.1732784G>T	NCBI36
NG_008655.1:g.14015C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.755C>A MANE Select	ENSP00000236671.2:p.Ser252Tyr
ENST00000367196.4:c.650C>A	ENSP00000356164.4:p.Ser217Tyr
ENST00000427721.3:c.180C>A
ENST00000429746.2:c.650C>A	ENSP00000402586.2:p.Ser217Tyr
ENST00000433655.6:c.755C>A	ENSP00000404902.1:p.Ser252Tyr
ENST00000438213.6:c.755C>A	ENSP00000415036.2:p.Ser252Tyr
ENST00000497544.3:n.371C>A
ENST00000636397.1:c.755C>A	ENSP00000489910.1:p.Ser252Tyr
ENST00000636571.1:c.734C>A	ENSP00000490770.1:p.Ser245Tyr
ENST00000636615.1:c.755C>A	ENSP00000490014.1:p.Ser252Tyr
ENST00000636843.1:c.749C>A	ENSP00000490897.1:p.Ser250Tyr
ENST00000637158.1:n.353C>A
ENST00000637381.2:n.3183C>A
ENST00000637387.1:c.755C>A	ENSP00000490598.1:p.Ser252Tyr
ENST00000637815.2:c.755C>A	ENSP00000490344.1:p.Ser252Tyr
ENST00000637915.1:c.755C>A	ENSP00000490471.1:p.Ser252Tyr
ENST00000637937.1:n.63C>A
ENST00000678991.1:c.*616C>A	ENSP00000503019.1:n.*616C>A
ENST00000236671.6:c.755C>A	ENSP00000236671.2:p.Ser252Tyr
ENST00000427721.2:c.155C>A	ENSP00000415840.2:p.Ser52Tyr
ENST00000433655.5:c.755C>A	ENSP00000404902.1:p.Ser252Tyr
ENST00000438213.5:c.710C>A	ENSP00000415036.1:p.Ser237Tyr
ENST00000497544.1:n.371C>A
NM_001909.4:c.755C>A	NP_001900.1:p.Ser252Tyr
NM_001909.5:c.755C>A MANE Select	NP_001900.1:p.Ser252Tyr