Canonical Allele Identifier: CA2746085238

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804104dup , CM000663.2:g.150804104dup	GRCh38
NC_000001.10:g.150776580dup , CM000663.1:g.150776580dup	GRCh37
NC_000001.9:g.149043204dup	NCBI36
NG_011848.1:g.9237dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.539dup MANE Select	ENSP00000271651.3:p.Tyr181LeufsTer16
ENST00000443913.2:c.716dup	ENSP00000405083.2:p.Tyr240LeufsTer16
ENST00000480670.2:n.3608dup
ENST00000676680.1:c.539dup	ENSP00000503270.1:p.Tyr181LeufsTer16
ENST00000676716.1:c.416dup	ENSP00000504737.1:p.Tyr140LeufsTer16
ENST00000676751.1:c.539dup	ENSP00000502964.1:p.Tyr181LeufsTer16
ENST00000676824.1:c.539dup	ENSP00000504176.1:p.Tyr181LeufsTer16
ENST00000676966.1:c.539dup	ENSP00000503723.1:p.Tyr181LeufsTer16
ENST00000676970.1:c.539dup	ENSP00000503832.1:p.Tyr181LeufsTer16
ENST00000677330.1:n.2365dup
ENST00000677611.1:n.391dup
ENST00000677887.1:c.581dup	ENSP00000503876.1:p.Tyr195LeufsTer16
ENST00000678275.1:c.*431dup	ENSP00000504796.1:n.*431dup
ENST00000678337.1:c.575dup	ENSP00000504759.1:p.Tyr193LeufsTer16
ENST00000678725.1:n.1516dup
ENST00000679090.1:n.1124dup
ENST00000679148.1:n.3501dup
ENST00000679171.1:n.2900dup
ENST00000679260.1:c.399+1761dup	ENSP00000504534.1:n.399+1761dup
ENST00000271651.7:c.539dup	ENSP00000271651.3:p.Tyr181LeufsTer16
ENST00000443913.1:c.716dup	ENSP00000405083.1:p.Tyr240LeufsTer16
ENST00000480670.1:n.379dup
NM_000396.3:c.539dup	NP_000387.1:p.Tyr181LeufsTer16
NM_000396.4:c.539dup MANE Select	NP_000387.1:p.Tyr181LeufsTer16