Canonical Allele Identifier: CA913325902

Gene: CTSK

Linked Data

• dbSNP Id: rs1557826730
• gnomAD v2: 1-150779055-AT-A
• gnomAD v3: 1-150806579-AT-A
• gnomAD v4: 1-150806579-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806582del , CM000663.2:g.150806582del	GRCh38
NC_000001.10:g.150779058del , CM000663.1:g.150779058del	GRCh37
NC_000001.9:g.149045682del	NCBI36
NG_011848.1:g.6757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.120+106del MANE Select	ENSP00000271651.3:n.120+106del
ENST00000443913.2:c.297+106del	ENSP00000405083.2:n.297+106del
ENST00000480670.2:n.2834del
ENST00000676680.1:c.120+106del	ENSP00000503270.1:n.120+106del
ENST00000676716.1:c.120+106del	ENSP00000504737.1:n.120+106del
ENST00000676751.1:c.120+106del	ENSP00000502964.1:n.120+106del
ENST00000676824.1:c.120+106del	ENSP00000504176.1:n.120+106del
ENST00000676966.1:c.120+106del	ENSP00000503723.1:n.120+106del
ENST00000676970.1:c.120+106del	ENSP00000503832.1:n.120+106del
ENST00000677330.1:n.1591del
ENST00000677887.1:c.162+106del	ENSP00000503876.1:n.162+106del
ENST00000678275.1:c.120+106del	ENSP00000504796.1:n.120+106del
ENST00000678337.1:c.156+106del	ENSP00000504759.1:n.156+106del
ENST00000678725.1:n.1097+106del
ENST00000679090.1:n.350del
ENST00000679148.1:n.1106del
ENST00000679171.1:n.2126del
ENST00000679260.1:c.120+106del	ENSP00000504534.1:n.120+106del
ENST00000271651.7:c.120+106del	ENSP00000271651.3:n.120+106del
ENST00000443913.1:c.297+106del	ENSP00000405083.1:n.297+106del
ENST00000480670.1:n.83+106del
NM_000396.3:c.120+106del	NP_000387.1:n.120+106del
NM_000396.4:c.120+106del MANE Select	NP_000387.1:n.120+106del