Canonical Allele Identifier: CA475929516

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88042352_88042354del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309188_88309190del , CM000673.2:g.88309188_88309190del	GRCh38
NC_000011.9:g.88042356_88042358del , CM000673.1:g.88042356_88042358del	GRCh37
NC_000011.8:g.87682004_87682006del	NCBI36
NG_007952.1:g.33588_33590del , LRG_50:g.33588_33590del

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.618_620del MANE Select	ENSP00000227266.4:p.Gly207del
ENST00000527018.6:c.618_620del	ENSP00000432556.2:p.Gly207del
ENST00000533897.2:n.666_668del
ENST00000676612.1:c.*425_*427del	ENSP00000504440.1:n.*425_*427del
ENST00000677208.1:c.*124_*126del	ENSP00000504347.1:n.*124_*126del
ENST00000677661.1:c.*295_*297del	ENSP00000503323.1:n.*295_*297del
ENST00000677802.1:c.*295_*297del	ENSP00000504115.1:n.*295_*297del
ENST00000678065.1:n.178_180del
ENST00000678395.1:c.*124_*126del	ENSP00000503123.1:n.*124_*126del
ENST00000678464.1:c.618_620del	ENSP00000503046.1:p.Gly207del
ENST00000678506.1:c.579_581del	ENSP00000503580.1:p.Gly194del
ENST00000678520.1:c.*292+3202_*292+3204del	ENSP00000503361.1:n.*292+3202_*292+3204de...
ENST00000678554.1:c.618_620del	ENSP00000504541.1:p.Gly207del
ENST00000678915.1:c.618_620del	ENSP00000504805.1:p.Gly207del
ENST00000679224.1:c.255_257del	ENSP00000504475.1:p.Gly86del
ENST00000227266.9:c.618_620del	ENSP00000227266.4:p.Gly207del
ENST00000527018.5:c.488_490del
NM_001814.4:c.618_620del , LRG_50t1:c.618_620del	NP_001805.3:p.Gly207del
NM_001814.5:c.618_620del	NP_001805.3:p.Gly207del
NM_001814.6:c.618_620del MANE Select	NP_001805.4:p.Gly207del