Canonical Allele Identifier: CA2574054763

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150803989C>T , CM000663.2:g.150803989C>T	GRCh38
NC_000001.10:g.150776465C>T , CM000663.1:g.150776465C>T	GRCh37
NC_000001.9:g.149043089C>T	NCBI36
NG_011848.1:g.9348G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.618+32G>A MANE Select	ENSP00000271651.3:n.618+32G>A
ENST00000443913.2:c.795+32G>A	ENSP00000405083.2:n.795+32G>A
ENST00000480670.2:n.3687+32G>A
ENST00000676680.1:c.618+32G>A	ENSP00000503270.1:n.618+32G>A
ENST00000676716.1:c.495+32G>A	ENSP00000504737.1:n.495+32G>A
ENST00000676751.1:c.618+32G>A	ENSP00000502964.1:n.618+32G>A
ENST00000676824.1:c.618+32G>A	ENSP00000504176.1:n.618+32G>A
ENST00000676966.1:c.618+32G>A	ENSP00000503723.1:n.618+32G>A
ENST00000676970.1:c.618+32G>A	ENSP00000503832.1:n.618+32G>A
ENST00000677330.1:n.2444+32G>A
ENST00000677611.1:n.470+32G>A
ENST00000677887.1:c.660+32G>A	ENSP00000503876.1:n.660+32G>A
ENST00000678275.1:c.*510+32G>A	ENSP00000504796.1:n.*510+32G>A
ENST00000678337.1:c.654+32G>A	ENSP00000504759.1:n.654+32G>A
ENST00000678725.1:n.1595+32G>A
ENST00000679090.1:n.1203+32G>A
ENST00000679148.1:n.3580+32G>A
ENST00000679171.1:n.2979+32G>A
ENST00000679260.1:c.399+1872G>A	ENSP00000504534.1:n.399+1872G>A
ENST00000271651.7:c.618+32G>A	ENSP00000271651.3:n.618+32G>A
NM_000396.3:c.618+32G>A	NP_000387.1:n.618+32G>A
NM_000396.4:c.618+32G>A MANE Select	NP_000387.1:n.618+32G>A