Canonical Allele Identifier: CA342336964

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150805926C>A , CM000663.2:g.150805926C>A	GRCh38
NC_000001.10:g.150778402C>A , CM000663.1:g.150778402C>A	GRCh37
NC_000001.9:g.149045026C>A	NCBI36
NG_011848.1:g.7411G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.334G>T MANE Select	NP_000387.1:p.Glu112Ter
ENST00000271651.8:c.334G>T MANE Select	ENSP00000271651.3:p.Glu112Ter
NM_000396.3:c.334G>T	NP_000387.1:p.Glu112Ter
ENST00000271651.7:c.334G>T	ENSP00000271651.3:p.Glu112Ter
ENST00000443913.1:c.511G>T	ENSP00000405083.1:p.Glu171Ter
ENST00000443913.2:c.511G>T	ENSP00000405083.2:p.Glu171Ter
ENST00000480670.1:n.174G>T
ENST00000480670.2:n.3403G>T
ENST00000676680.1:c.334G>T	ENSP00000503270.1:p.Glu112Ter
ENST00000676716.1:c.211G>T	ENSP00000504737.1:p.Glu71Ter
ENST00000676751.1:c.334G>T	ENSP00000502964.1:p.Glu112Ter
ENST00000676824.1:c.334G>T	ENSP00000504176.1:p.Glu112Ter
ENST00000676966.1:c.334G>T	ENSP00000503723.1:p.Glu112Ter
ENST00000676970.1:c.334G>T	ENSP00000503832.1:p.Glu112Ter
ENST00000677330.1:n.2160G>T
ENST00000677611.1:n.186G>T
ENST00000677887.1:c.376G>T	ENSP00000503876.1:p.Glu126Ter
ENST00000678275.1:c.*226G>T	ENSP00000504796.1:n.*226G>T
ENST00000678337.1:c.370G>T	ENSP00000504759.1:p.Glu124Ter
ENST00000678725.1:n.1311G>T
ENST00000679090.1:n.919G>T
ENST00000679148.1:n.1675G>T
ENST00000679171.1:n.2695G>T
ENST00000679260.1:c.334G>T	ENSP00000504534.1:p.Glu112Ter