Canonical Allele Identifier: CA379092884

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1775055G>T (hg19) ; chr11:g.1753825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753825G>T , CM000673.2:g.1753825G>T	GRCh38
NC_000011.9:g.1775055G>T , CM000673.1:g.1775055G>T	GRCh37
NC_000011.8:g.1731631G>T	NCBI36
NG_008655.1:g.15168C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1049C>A MANE Select	ENSP00000236671.2:p.Ser350Tyr
ENST00000367196.4:c.944C>A	ENSP00000356164.4:p.Ser315Tyr
ENST00000427721.3:c.474C>A
ENST00000429746.2:c.944C>A	ENSP00000402586.2:p.Ser315Tyr
ENST00000433655.6:c.*215C>A	ENSP00000404902.1:n.*215C>A
ENST00000438213.6:c.1166C>A	ENSP00000415036.2:p.Ser389Tyr
ENST00000497544.3:n.757C>A
ENST00000636397.1:c.1049C>A	ENSP00000489910.1:p.Ser350Tyr
ENST00000636571.1:c.1028C>A	ENSP00000490770.1:p.Ser343Tyr
ENST00000636579.1:c.50C>A	ENSP00000490489.1:p.Ser17Tyr
ENST00000636615.1:c.1049C>A	ENSP00000490014.1:p.Ser350Tyr
ENST00000636843.1:c.1043C>A	ENSP00000490897.1:p.Ser348Tyr
ENST00000637158.1:n.647C>A
ENST00000637381.2:n.3477C>A
ENST00000637387.1:c.1028C>A	ENSP00000490598.1:p.Ser343Tyr
ENST00000637815.2:c.1031C>A	ENSP00000490344.1:p.Ser344Tyr
ENST00000637915.1:c.1049C>A	ENSP00000490471.1:p.Ser350Tyr
ENST00000637937.1:n.357C>A
ENST00000678991.1:c.*910C>A	ENSP00000503019.1:n.*910C>A
ENST00000236671.6:c.1049C>A	ENSP00000236671.2:p.Ser350Tyr
ENST00000427721.2:c.449C>A	ENSP00000415840.2:p.Ser150Tyr
ENST00000429746.1:c.380C>A	ENSP00000402586.1:p.Ser127Tyr
ENST00000433655.5:c.*215C>A	ENSP00000404902.1:n.*215C>A
ENST00000497544.1:n.757C>A
NM_001909.4:c.1049C>A	NP_001900.1:p.Ser350Tyr
NM_001909.5:c.1049C>A MANE Select	NP_001900.1:p.Ser350Tyr