Canonical Allele Identifier: CA1080525

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150805896G>A , CM000663.2:g.150805896G>A	GRCh38
NC_000001.10:g.150778372G>A , CM000663.1:g.150778372G>A	GRCh37
NC_000001.9:g.149044996G>A	NCBI36
NG_011848.1:g.7441C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.364C>T MANE Select	NP_000387.1:p.Arg122Ter
ENST00000271651.8:c.364C>T MANE Select	ENSP00000271651.3:p.Arg122Ter
NM_000396.3:c.364C>T	NP_000387.1:p.Arg122Ter
ENST00000271651.7:c.364C>T	ENSP00000271651.3:p.Arg122Ter
ENST00000443913.1:c.541C>T	ENSP00000405083.1:p.Arg181Ter
ENST00000443913.2:c.541C>T	ENSP00000405083.2:p.Arg181Ter
ENST00000480670.1:n.204C>T
ENST00000480670.2:n.3433C>T
ENST00000676680.1:c.364C>T	ENSP00000503270.1:p.Arg122Ter
ENST00000676716.1:c.241C>T	ENSP00000504737.1:p.Arg81Ter
ENST00000676751.1:c.364C>T	ENSP00000502964.1:p.Arg122Ter
ENST00000676824.1:c.364C>T	ENSP00000504176.1:p.Arg122Ter
ENST00000676966.1:c.364C>T	ENSP00000503723.1:p.Arg122Ter
ENST00000676970.1:c.364C>T	ENSP00000503832.1:p.Arg122Ter
ENST00000677330.1:n.2190C>T
ENST00000677611.1:n.216C>T
ENST00000677887.1:c.406C>T	ENSP00000503876.1:p.Arg136Ter
ENST00000678275.1:c.*256C>T	ENSP00000504796.1:n.*256C>T
ENST00000678337.1:c.400C>T	ENSP00000504759.1:p.Arg134Ter
ENST00000678725.1:n.1341C>T
ENST00000679090.1:n.949C>T
ENST00000679148.1:n.1705C>T
ENST00000679171.1:n.2725C>T
ENST00000679260.1:c.364C>T	ENSP00000504534.1:p.Arg122Ter