Canonical Allele Identifier: CA342335944

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799543C>T , CM000663.2:g.150799543C>T	GRCh38
NC_000001.10:g.150772019C>T , CM000663.1:g.150772019C>T	GRCh37
NC_000001.9:g.149038643C>T	NCBI36
NG_011848.1:g.13794G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.784+1G>A MANE Select	NP_000387.1:n.784+1G>A
ENST00000271651.8:c.784+1G>A MANE Select	ENSP00000271651.3:n.784+1G>A
NM_000396.3:c.784+1G>A	NP_000387.1:n.784+1G>A
ENST00000271651.7:c.784+1G>A	ENSP00000271651.3:n.784+1G>A
ENST00000443913.2:c.961+1G>A	ENSP00000405083.2:n.961+1G>A
ENST00000480670.2:n.3853+1G>A
ENST00000676680.1:c.*78+1G>A	ENSP00000503270.1:n.*78+1G>A
ENST00000676716.1:c.661+1G>A	ENSP00000504737.1:n.661+1G>A
ENST00000676751.1:c.784+1G>A	ENSP00000502964.1:n.784+1G>A
ENST00000676824.1:c.784+1G>A	ENSP00000504176.1:n.784+1G>A
ENST00000676966.1:c.784+1G>A	ENSP00000503723.1:n.784+1G>A
ENST00000676970.1:c.784+1G>A	ENSP00000503832.1:n.784+1G>A
ENST00000677330.1:n.2610+1G>A
ENST00000677611.1:n.636+1G>A
ENST00000677887.1:c.826+1G>A	ENSP00000503876.1:n.826+1G>A
ENST00000678275.1:c.*676+1G>A	ENSP00000504796.1:n.*676+1G>A
ENST00000678337.1:c.820+1G>A	ENSP00000504759.1:n.820+1G>A
ENST00000678725.1:n.1762G>A
ENST00000679090.1:n.1370G>A
ENST00000679148.1:n.3746+1G>A
ENST00000679171.1:n.3146G>A
ENST00000679178.1:n.495+1G>A
ENST00000679260.1:c.565+1G>A	ENSP00000504534.1:n.565+1G>A