Canonical Allele Identifier: CA379092428

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774793G>C (hg19) ; chr11:g.1753563G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753563G>C , CM000673.2:g.1753563G>C	GRCh38
NC_000011.9:g.1774793G>C , CM000673.1:g.1774793G>C	GRCh37
NC_000011.8:g.1731369G>C	NCBI36
NG_008655.1:g.15430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1179C>G MANE Select	ENSP00000236671.2:p.Tyr393Ter
ENST00000367196.4:c.1074C>G	ENSP00000356164.4:p.Tyr358Ter
ENST00000427721.3:c.604C>G
ENST00000429746.2:c.1074C>G	ENSP00000402586.2:p.Tyr358Ter
ENST00000433655.6:c.*345C>G	ENSP00000404902.1:n.*345C>G
ENST00000438213.6:c.1296C>G	ENSP00000415036.2:p.Tyr432Ter
ENST00000636397.1:c.1071+240C>G	ENSP00000489910.1:n.1071+240C>G
ENST00000636571.1:c.1158C>G	ENSP00000490770.1:p.Tyr386Ter
ENST00000636579.1:c.72+240C>G	ENSP00000490489.1:n.72+240C>G
ENST00000636615.1:c.1071+240C>G	ENSP00000490014.1:n.1071+240C>G
ENST00000636843.1:c.1173C>G	ENSP00000490897.1:p.Tyr391Ter
ENST00000637158.1:n.777C>G
ENST00000637381.2:n.3607C>G
ENST00000637387.1:c.1158C>G	ENSP00000490598.1:p.Tyr386Ter
ENST00000637815.2:c.1161C>G	ENSP00000490344.1:p.Tyr387Ter
ENST00000637915.1:c.1170C>G	ENSP00000490471.1:p.Tyr390Ter
ENST00000637937.1:n.487C>G
ENST00000678991.1:c.*1040C>G	ENSP00000503019.1:n.*1040C>G
ENST00000236671.6:c.1179C>G	ENSP00000236671.2:p.Tyr393Ter
ENST00000427721.2:c.471+240C>G	ENSP00000415840.2:n.471+240C>G
ENST00000429746.1:c.510C>G	ENSP00000402586.1:p.Tyr170Ter
ENST00000433655.5:c.*345C>G	ENSP00000404902.1:n.*345C>G
NM_001909.4:c.1179C>G	NP_001900.1:p.Tyr393Ter
NM_001909.5:c.1179C>G MANE Select	NP_001900.1:p.Tyr393Ter