Canonical Allele Identifier: CA342336214

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799670T>A , CM000663.2:g.150799670T>A	GRCh38
NC_000001.10:g.150772146T>A , CM000663.1:g.150772146T>A	GRCh37
NC_000001.9:g.149038770T>A	NCBI36
NG_011848.1:g.13667A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.658A>T MANE Select	NP_000387.1:p.Lys220Ter
ENST00000271651.8:c.658A>T MANE Select	ENSP00000271651.3:p.Lys220Ter
NM_000396.3:c.658A>T	NP_000387.1:p.Lys220Ter
ENST00000271651.7:c.658A>T	ENSP00000271651.3:p.Lys220Ter
ENST00000443913.2:c.835A>T	ENSP00000405083.2:p.Lys279Ter
ENST00000480670.2:n.3727A>T
ENST00000676680.1:c.654A>T	ENSP00000503270.1:p.Leu218=
ENST00000676716.1:c.535A>T	ENSP00000504737.1:p.Lys179Ter
ENST00000676751.1:c.658A>T	ENSP00000502964.1:p.Lys220Ter
ENST00000676824.1:c.658A>T	ENSP00000504176.1:p.Lys220Ter
ENST00000676966.1:c.658A>T	ENSP00000503723.1:p.Lys220Ter
ENST00000676970.1:c.658A>T	ENSP00000503832.1:p.Lys220Ter
ENST00000677330.1:n.2484A>T
ENST00000677611.1:n.510A>T
ENST00000677887.1:c.700A>T	ENSP00000503876.1:p.Lys234Ter
ENST00000678275.1:c.*550A>T	ENSP00000504796.1:n.*550A>T
ENST00000678337.1:c.694A>T	ENSP00000504759.1:p.Lys232Ter
ENST00000678725.1:n.1635A>T
ENST00000679090.1:n.1243A>T
ENST00000679148.1:n.3620A>T
ENST00000679171.1:n.3019A>T
ENST00000679178.1:n.369A>T
ENST00000679260.1:c.439A>T	ENSP00000504534.1:p.Lys147Ter