Canonical Allele Identifier: CA2479315139

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806579_150806580delinsAT , CM000663.2:g.150806579_150806580delinsAT	GRCh38
NC_000001.10:g.150779055_150779056delinsAT , CM000663.1:g.150779055_150779056delinsAT	GRCh37
NC_000001.9:g.149045679_149045680delinsAT	NCBI36
NG_011848.1:g.6757_6758delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.120+106_120+107delinsAT MANE Select	ENSP00000271651.3:n.120+106_120+107delinsAT
ENST00000443913.2:c.297+106_297+107delinsAT	ENSP00000405083.2:n.297+106_297+107delinsAT
ENST00000480670.2:n.2834_2835delinsAT
ENST00000676680.1:c.120+106_120+107delinsAT	ENSP00000503270.1:n.120+106_120+107delinsAT
ENST00000676716.1:c.120+106_120+107delinsAT	ENSP00000504737.1:n.120+106_120+107delinsAT
ENST00000676751.1:c.120+106_120+107delinsAT	ENSP00000502964.1:n.120+106_120+107delinsAT
ENST00000676824.1:c.120+106_120+107delinsAT	ENSP00000504176.1:n.120+106_120+107delinsAT
ENST00000676966.1:c.120+106_120+107delinsAT	ENSP00000503723.1:n.120+106_120+107delinsAT
ENST00000676970.1:c.120+106_120+107delinsAT	ENSP00000503832.1:n.120+106_120+107delinsAT
ENST00000677330.1:n.1591_1592delinsAT
ENST00000677887.1:c.162+106_162+107delinsAT	ENSP00000503876.1:n.162+106_162+107delinsAT
ENST00000678275.1:c.120+106_120+107delinsAT	ENSP00000504796.1:n.120+106_120+107delinsAT
ENST00000678337.1:c.156+106_156+107delinsAT	ENSP00000504759.1:n.156+106_156+107delinsAT
ENST00000678725.1:n.1097+106_1097+107delinsAT
ENST00000679090.1:n.350_351delinsAT
ENST00000679148.1:n.1106_1107delinsAT
ENST00000679171.1:n.2126_2127delinsAT
ENST00000679260.1:c.120+106_120+107delinsAT	ENSP00000504534.1:n.120+106_120+107delinsAT
ENST00000271651.7:c.120+106_120+107delinsAT	ENSP00000271651.3:n.120+106_120+107delinsAT
ENST00000443913.1:c.297+106_297+107delinsAT	ENSP00000405083.1:n.297+106_297+107delinsAT
ENST00000480670.1:n.83+106_83+107delinsAT
NM_000396.3:c.120+106_120+107delinsAT	NP_000387.1:n.120+106_120+107delinsAT
NM_000396.4:c.120+106_120+107delinsAT MANE Select	NP_000387.1:n.120+106_120+107delinsAT