Canonical Allele Identifier: CA472140827

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774880G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753650G>C , CM000673.2:g.1753650G>C	GRCh38
NC_000011.9:g.1774880G>C , CM000673.1:g.1774880G>C	GRCh37
NC_000011.8:g.1731456G>C	NCBI36
NG_008655.1:g.15343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1092C>G MANE Select	ENSP00000236671.2:p.Thr364=
ENST00000367196.4:c.987C>G	ENSP00000356164.4:p.Thr329=
ENST00000427721.3:c.517C>G
ENST00000429746.2:c.987C>G	ENSP00000402586.2:p.Thr329=
ENST00000433655.6:c.*258C>G	ENSP00000404902.1:n.*258C>G
ENST00000438213.6:c.1209C>G	ENSP00000415036.2:p.Thr403=
ENST00000636397.1:c.1071+153C>G	ENSP00000489910.1:n.1071+153C>G
ENST00000636571.1:c.1071C>G	ENSP00000490770.1:p.Thr357=
ENST00000636579.1:c.72+153C>G	ENSP00000490489.1:n.72+153C>G
ENST00000636615.1:c.1071+153C>G	ENSP00000490014.1:n.1071+153C>G
ENST00000636843.1:c.1086C>G	ENSP00000490897.1:p.Thr362=
ENST00000637158.1:n.690C>G
ENST00000637381.2:n.3520C>G
ENST00000637387.1:c.1071C>G	ENSP00000490598.1:p.Thr357=
ENST00000637815.2:c.1074C>G	ENSP00000490344.1:p.Thr358=
ENST00000637915.1:c.1083C>G	ENSP00000490471.1:p.Thr361=
ENST00000637937.1:n.400C>G
ENST00000678991.1:c.*953C>G	ENSP00000503019.1:n.*953C>G
ENST00000236671.6:c.1092C>G	ENSP00000236671.2:p.Thr364=
ENST00000427721.2:c.471+153C>G	ENSP00000415840.2:n.471+153C>G
ENST00000429746.1:c.423C>G	ENSP00000402586.1:p.Thr141=
ENST00000433655.5:c.*258C>G	ENSP00000404902.1:n.*258C>G
NM_001909.4:c.1092C>G	NP_001900.1:p.Thr364=
NM_001909.5:c.1092C>G MANE Select	NP_001900.1:p.Thr364=