Canonical Allele Identifier: CA1080394

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796881C>T , CM000663.2:g.150796881C>T	GRCh38
NC_000001.10:g.150769357C>T , CM000663.1:g.150769357C>T	GRCh37
NC_000001.9:g.149035981C>T	NCBI36
NG_011848.1:g.16456G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.908G>A MANE Select	NP_000387.1:p.Gly303Glu
ENST00000271651.8:c.908G>A MANE Select	ENSP00000271651.3:p.Gly303Glu
NM_000396.3:c.908G>A	NP_000387.1:p.Gly303Glu
ENST00000271651.7:c.908G>A	ENSP00000271651.3:p.Gly303Glu
ENST00000443913.2:c.1085G>A	ENSP00000405083.2:p.Gly362Glu
ENST00000480670.2:n.3977G>A
ENST00000676680.1:c.*202G>A	ENSP00000503270.1:n.*202G>A
ENST00000676716.1:c.785G>A	ENSP00000504737.1:p.Gly262Glu
ENST00000676751.1:c.802G>A	ENSP00000502964.1:p.Glu268Lys
ENST00000676824.1:c.908G>A	ENSP00000504176.1:p.Gly303Glu
ENST00000676966.1:c.908G>A	ENSP00000503723.1:p.Gly303Glu
ENST00000676970.1:c.920G>A	ENSP00000503832.1:p.Gly307Glu
ENST00000677330.1:n.2734G>A
ENST00000677611.1:n.760G>A
ENST00000677887.1:c.950G>A	ENSP00000503876.1:p.Gly317Glu
ENST00000678275.1:c.*800G>A	ENSP00000504796.1:n.*800G>A
ENST00000678337.1:c.944G>A	ENSP00000504759.1:p.Gly315Glu
ENST00000678725.1:n.2155G>A
ENST00000679090.1:n.1763G>A
ENST00000679148.1:n.3870G>A
ENST00000679171.1:n.3539G>A
ENST00000679178.1:n.619G>A
ENST00000679260.1:c.689G>A	ENSP00000504534.1:p.Gly230Glu