Canonical Allele Identifier: CA2479315174

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806680_150806681delinsAG , CM000663.2:g.150806680_150806681delinsAG	GRCh38
NC_000001.10:g.150779156_150779157delinsAG , CM000663.1:g.150779156_150779157delinsAG	GRCh37
NC_000001.9:g.149045780_149045781delinsAG	NCBI36
NG_011848.1:g.6656_6657delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.120+5_120+6delinsCT MANE Select	ENSP00000271651.3:n.120+5_120+6delinsCT
ENST00000443913.2:c.297+5_297+6delinsCT	ENSP00000405083.2:n.297+5_297+6delinsCT
ENST00000480670.2:n.2733_2734delinsCT
ENST00000676680.1:c.120+5_120+6delinsCT	ENSP00000503270.1:n.120+5_120+6delinsCT
ENST00000676716.1:c.120+5_120+6delinsCT	ENSP00000504737.1:n.120+5_120+6delinsCT
ENST00000676751.1:c.120+5_120+6delinsCT	ENSP00000502964.1:n.120+5_120+6delinsCT
ENST00000676824.1:c.120+5_120+6delinsCT	ENSP00000504176.1:n.120+5_120+6delinsCT
ENST00000676966.1:c.120+5_120+6delinsCT	ENSP00000503723.1:n.120+5_120+6delinsCT
ENST00000676970.1:c.120+5_120+6delinsCT	ENSP00000503832.1:n.120+5_120+6delinsCT
ENST00000677330.1:n.1490_1491delinsCT
ENST00000677887.1:c.162+5_162+6delinsCT	ENSP00000503876.1:n.162+5_162+6delinsCT
ENST00000678275.1:c.120+5_120+6delinsCT	ENSP00000504796.1:n.120+5_120+6delinsCT
ENST00000678337.1:c.156+5_156+6delinsCT	ENSP00000504759.1:n.156+5_156+6delinsCT
ENST00000678725.1:n.1097+5_1097+6delinsCT
ENST00000679090.1:n.249_250delinsCT
ENST00000679148.1:n.1005_1006delinsCT
ENST00000679171.1:n.2025_2026delinsCT
ENST00000679260.1:c.120+5_120+6delinsCT	ENSP00000504534.1:n.120+5_120+6delinsCT
ENST00000271651.7:c.120+5_120+6delinsCT	ENSP00000271651.3:n.120+5_120+6delinsCT
ENST00000443913.1:c.297+5_297+6delinsCT	ENSP00000405083.1:n.297+5_297+6delinsCT
ENST00000480670.1:n.83+5_83+6delinsCT
NM_000396.3:c.120+5_120+6delinsCT	NP_000387.1:n.120+5_120+6delinsCT
NM_000396.4:c.120+5_120+6delinsCT MANE Select	NP_000387.1:n.120+5_120+6delinsCT