Canonical Allele Identifier: CA342335833

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799231T>C , CM000663.2:g.150799231T>C	GRCh38
NC_000001.10:g.150771707T>C , CM000663.1:g.150771707T>C	GRCh37
NC_000001.9:g.149038331T>C	NCBI36
NG_011848.1:g.14106A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.827A>G MANE Select	NP_000387.1:p.His276Arg
ENST00000271651.8:c.827A>G MANE Select	ENSP00000271651.3:p.His276Arg
NM_000396.3:c.827A>G	NP_000387.1:p.His276Arg
ENST00000271651.7:c.827A>G	ENSP00000271651.3:p.His276Arg
ENST00000443913.2:c.1004A>G	ENSP00000405083.2:p.His335Arg
ENST00000480670.2:n.3896A>G
ENST00000676680.1:c.*121A>G	ENSP00000503270.1:n.*121A>G
ENST00000676716.1:c.704A>G	ENSP00000504737.1:p.His235Arg
ENST00000676751.1:c.784+313A>G	ENSP00000502964.1:n.784+313A>G
ENST00000676824.1:c.827A>G	ENSP00000504176.1:p.His276Arg
ENST00000676966.1:c.827A>G	ENSP00000503723.1:p.His276Arg
ENST00000676970.1:c.839A>G	ENSP00000503832.1:p.His280Arg
ENST00000677330.1:n.2653A>G
ENST00000677611.1:n.679A>G
ENST00000677887.1:c.869A>G	ENSP00000503876.1:p.His290Arg
ENST00000678275.1:c.*719A>G	ENSP00000504796.1:n.*719A>G
ENST00000678337.1:c.863A>G	ENSP00000504759.1:p.His288Arg
ENST00000678725.1:n.2074A>G
ENST00000679090.1:n.1682A>G
ENST00000679148.1:n.3789A>G
ENST00000679171.1:n.3458A>G
ENST00000679178.1:n.538A>G
ENST00000679260.1:c.608A>G	ENSP00000504534.1:p.His203Arg