Canonical Allele Identifier: CA342335587

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796863A>T , CM000663.2:g.150796863A>T	GRCh38
NC_000001.10:g.150769339A>T , CM000663.1:g.150769339A>T	GRCh37
NC_000001.9:g.149035963A>T	NCBI36
NG_011848.1:g.16474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.926T>A MANE Select	ENSP00000271651.3:p.Leu309His
ENST00000443913.2:c.1103T>A	ENSP00000405083.2:p.Leu368His
ENST00000480670.2:n.3995T>A
ENST00000676680.1:c.*220T>A	ENSP00000503270.1:n.*220T>A
ENST00000676716.1:c.803T>A	ENSP00000504737.1:p.Leu268His
ENST00000676751.1:c.820T>A	ENSP00000502964.1:p.Ser274Thr
ENST00000676824.1:c.926T>A	ENSP00000504176.1:p.Leu309His
ENST00000676966.1:c.926T>A	ENSP00000503723.1:p.Leu309His
ENST00000676970.1:c.938T>A	ENSP00000503832.1:p.Leu313His
ENST00000677330.1:n.2752T>A
ENST00000677611.1:n.778T>A
ENST00000677887.1:c.968T>A	ENSP00000503876.1:p.Leu323His
ENST00000678275.1:c.*818T>A	ENSP00000504796.1:n.*818T>A
ENST00000678337.1:c.962T>A	ENSP00000504759.1:p.Leu321His
ENST00000678725.1:n.2173T>A
ENST00000679090.1:n.1781T>A
ENST00000679148.1:n.3888T>A
ENST00000679171.1:n.3557T>A
ENST00000679178.1:n.637T>A
ENST00000679260.1:c.707T>A	ENSP00000504534.1:p.Leu236His
ENST00000271651.7:c.926T>A	ENSP00000271651.3:p.Leu309His
NM_000396.3:c.926T>A	NP_000387.1:p.Leu309His
NM_000396.4:c.926T>A MANE Select	NP_000387.1:p.Leu309His