Canonical Allele Identifier: CA2615475883

Gene: CTSC

Linked Data

• gnomAD v4: 11-88312543-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312548_88312550del , CM000673.2:g.88312548_88312550del	GRCh38
NC_000011.9:g.88045716_88045718del , CM000673.1:g.88045716_88045718del	GRCh37
NC_000011.8:g.87685364_87685366del	NCBI36
NG_007952.1:g.30228_30230del , LRG_50:g.30228_30230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.327_329del MANE Select	ENSP00000227266.4:p.Glu110del
ENST00000527018.6:c.327_329del	ENSP00000432556.2:p.Glu110del
ENST00000533897.2:n.375_377del
ENST00000676612.1:c.*134_*136del	ENSP00000504440.1:n.*134_*136del
ENST00000677208.1:c.319-3228_319-3226del	ENSP00000504347.1:n.319-3228_319-3226del
ENST00000677661.1:c.*4_*6del	ENSP00000503323.1:n.*4_*6del
ENST00000677802.1:c.*4_*6del	ENSP00000504115.1:n.*4_*6del
ENST00000678395.1:c.327_329del	ENSP00000503123.1:p.Glu110del
ENST00000678464.1:c.327_329del	ENSP00000503046.1:p.Glu110del
ENST00000678506.1:c.327_329del	ENSP00000503580.1:p.Glu110del
ENST00000678520.1:c.*134_*136del	ENSP00000503361.1:n.*134_*136del
ENST00000678554.1:c.327_329del	ENSP00000504541.1:p.Glu110del
ENST00000678915.1:c.327_329del	ENSP00000504805.1:p.Glu110del
ENST00000679224.1:c.-37_-35del	ENSP00000504475.1:n.-37_-35del
ENST00000227266.9:c.327_329del	ENSP00000227266.4:p.Glu110del
ENST00000527018.5:c.197_199del
ENST00000533865.5:n.349_351del
NM_001814.4:c.327_329del , LRG_50t1:c.327_329del	NP_001805.3:p.Glu110del
NM_001814.5:c.327_329del	NP_001805.3:p.Glu110del
NM_001814.6:c.327_329del MANE Select	NP_001805.4:p.Glu110del