Canonical Allele Identifier: CA379092403

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774782A>G (hg19) ; chr11:g.1753552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753552A>G , CM000673.2:g.1753552A>G	GRCh38
NC_000011.9:g.1774782A>G , CM000673.1:g.1774782A>G	GRCh37
NC_000011.8:g.1731358A>G	NCBI36
NG_008655.1:g.15441T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1190T>C MANE Select	ENSP00000236671.2:p.Phe397Ser
ENST00000367196.4:c.1085T>C	ENSP00000356164.4:p.Phe362Ser
ENST00000427721.3:c.615T>C
ENST00000429746.2:c.1085T>C	ENSP00000402586.2:p.Phe362Ser
ENST00000433655.6:c.*356T>C	ENSP00000404902.1:n.*356T>C
ENST00000438213.6:c.1307T>C	ENSP00000415036.2:p.Phe436Ser
ENST00000636397.1:c.1071+251T>C	ENSP00000489910.1:n.1071+251T>C
ENST00000636571.1:c.1169T>C	ENSP00000490770.1:p.Phe390Ser
ENST00000636579.1:c.72+251T>C	ENSP00000490489.1:n.72+251T>C
ENST00000636615.1:c.1071+251T>C	ENSP00000490014.1:n.1071+251T>C
ENST00000636843.1:c.1184T>C	ENSP00000490897.1:p.Phe395Ser
ENST00000637158.1:n.788T>C
ENST00000637381.2:n.3618T>C
ENST00000637387.1:c.1169T>C	ENSP00000490598.1:p.Phe390Ser
ENST00000637815.2:c.1172T>C	ENSP00000490344.1:p.Phe391Ser
ENST00000637915.1:c.1181T>C	ENSP00000490471.1:p.Phe394Ser
ENST00000637937.1:n.498T>C
ENST00000678991.1:c.*1051T>C	ENSP00000503019.1:n.*1051T>C
ENST00000236671.6:c.1190T>C	ENSP00000236671.2:p.Phe397Ser
ENST00000427721.2:c.471+251T>C	ENSP00000415840.2:n.471+251T>C
ENST00000429746.1:c.521T>C	ENSP00000402586.1:p.Phe174Ser
ENST00000433655.5:c.*356T>C	ENSP00000404902.1:n.*356T>C
NM_001909.4:c.1190T>C	NP_001900.1:p.Phe397Ser
NM_001909.5:c.1190T>C MANE Select	NP_001900.1:p.Phe397Ser