Canonical Allele Identifier: CA600764765

Gene: CTSC

Linked Data

• dbSNP Id: rs1443528055
• gnomAD v2: 11-88033672-CA-C
• gnomAD v4: 11-88300504-CA-C
• MyVariant Identifiers: chr11:g.88033673del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88300510del , CM000673.2:g.88300510del	GRCh38
NC_000011.9:g.88033678del , CM000673.1:g.88033678del	GRCh37
NC_000011.8:g.87673326del	NCBI36
NG_007952.1:g.42269del , LRG_50:g.42269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.757+25del MANE Select	ENSP00000227266.4:n.757+25del
ENST00000527018.6:c.757+25del	ENSP00000432556.2:n.757+25del
ENST00000533897.2:n.830del
ENST00000676612.1:c.*564+25del	ENSP00000504440.1:n.*564+25del
ENST00000677208.1:c.*263+25del	ENSP00000504347.1:n.*263+25del
ENST00000677661.1:c.*434+25del	ENSP00000503323.1:n.*434+25del
ENST00000677802.1:c.*434+25del	ENSP00000504115.1:n.*434+25del
ENST00000678065.1:n.342del
ENST00000678395.1:c.*263+25del	ENSP00000503123.1:n.*263+25del
ENST00000678464.1:c.757+25del	ENSP00000503046.1:n.757+25del
ENST00000678506.1:c.718+25del	ENSP00000503580.1:n.718+25del
ENST00000678520.1:c.*408+25del	ENSP00000503361.1:n.*408+25del
ENST00000678554.1:c.757+25del	ENSP00000504541.1:n.757+25del
ENST00000678915.1:c.757+25del	ENSP00000504805.1:n.757+25del
ENST00000679224.1:c.394+25del	ENSP00000504475.1:n.394+25del
ENST00000227266.9:c.757+25del	ENSP00000227266.4:n.757+25del
ENST00000527018.5:c.627+25del
NM_001814.4:c.757+25del , LRG_50t1:c.757+25del	NP_001805.3:n.757+25del
NM_001814.5:c.757+25del	NP_001805.3:n.757+25del
NM_001814.6:c.757+25del MANE Select	NP_001805.4:n.757+25del