Canonical Allele Identifier: CA2536372635

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798681_47798682insACTGTTTT , CM000664.2:g.47798681_47798682insACTGTTTT	GRCh38
NC_000002.11:g.48025820_48025821insACTGTTTT , CM000664.1:g.48025820_48025821insACTGTTTT	GRCh37
NC_000002.10:g.47879324_47879325insACTGTTTT	NCBI36
NG_007111.1:g.20535_20536insACTGTTTT , LRG_219:g.20535_20536insACTGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.401_402insACTGTTTT (MSH6)	ENSP00000406248.2:p.Lys135LeufsTer15
ENST00000420813.6:c.401_402insACTGTTTT (MSH6)	ENSP00000390382.2:p.Lys135LeufsTer15
ENST00000455383.6:c.401_402insACTGTTTT (MSH6)	ENSP00000397484.2:p.Lys135LeufsTer15
ENST00000700004.2:c.698_699insACTGTTTT (MSH6)	ENSP00000514752.2:p.Lys234LeufsTer15
ENST00000699999.1:n.782_783insACTGTTTT (MSH6)
ENST00000700000.1:c.698_699insACTGTTTT (MSH6)	ENSP00000514749.1:p.Lys234LeufsTer15
ENST00000700002.1:c.704_705insACTGTTTT (MSH6)	ENSP00000514750.1:p.Lys236LeufsTer15
ENST00000700003.1:c.627+2618_627+2619insACTGTTTT (MSH6)	ENSP00000514751.1:n.627+2618_627+2619insACTGTTTT
ENST00000234420.11:c.698_699insACTGTTTT (MSH6) MANE Select	ENSP00000234420.5:p.Lys234LeufsTer15
ENST00000540021.6:c.308_309insACTGTTTT (MSH6)	ENSP00000446475.1:p.Lys104LeufsTer15
ENST00000652107.1:c.401_402insACTGTTTT (MSH6)	ENSP00000498629.1:p.Lys135LeufsTer15
ENST00000673637.1:c.401_402insACTGTTTT (MSH6)	ENSP00000501310.1:p.Lys135LeufsTer15
ENST00000673922.1:n.420_421insACTGTTTT (MSH6)
ENST00000234420.9:c.698_699insACTGTTTT (MSH6)	ENSP00000234420.4:p.Lys234LeufsTer15
ENST00000405808.5:c.170-9242_170-9241insAAAACAGT (FBXO11)	ENSP00000385127.1:n.170-9242_170-9241insAAAACAGT
ENST00000411819.1:c.401_402insACTGTTTT (MSH6)	ENSP00000406248.1:p.Lys135LeufsTer15
ENST00000434234.5:c.*125-9242_*125-9241insAAAACAGT (FBXO11)	ENSP00000402692.1:n.*125-9242_*125-9241insAAAACAGT
ENST00000445503.5:c.*45_*46insACTGTTTT (MSH6)	ENSP00000405294.1:n.*45_*46insACTGTTTT
ENST00000456246.1:c.*186_*187insACTGTTTT (MSH6)	ENSP00000410570.1:n.*186_*187insACTGTTTT
ENST00000538136.1:c.-209_-208insACTGTTTT (MSH6)	ENSP00000438580.1:n.-209_-208insACTGTTTT
ENST00000540021.5:c.308_309insACTGTTTT (MSH6)	ENSP00000446475.1:p.Lys104LeufsTer15
ENST00000614496.4:c.-209_-208insACTGTTTT (MSH6)	ENSP00000477844.1:n.-209_-208insACTGTTTT
ENST00000616033.4:c.695_696insACTGTTTT (MSH6)	ENSP00000480261.1:p.Lys233LeufsTer15
ENST00000622629.4:c.-2399_-2398insACTGTTTT (MSH6)	ENSP00000482078.1:n.-2399_-2398insACTGTTTT
NM_000179.2:c.698_699insACTGTTTT , LRG_219t1:c.698_699insACTGTTTT (MSH6)	NP_000170.1:p.Lys234LeufsTer15
NM_001281492.1:c.308_309insACTGTTTT (MSH6)	NP_001268421.1:p.Lys104LeufsTer15
NM_001281493.1:c.-209_-208insACTGTTTT (MSH6)	NP_001268422.1:n.-209_-208insACTGTTTT
NM_001281494.1:c.-209_-208insACTGTTTT (MSH6)	NP_001268423.1:n.-209_-208insACTGTTTT
XM_005264271.1:c.401_402insACTGTTTT (MSH6)	XP_005264328.1:p.Lys135LeufsTer15
XM_011532798.1:c.515_516insACTGTTTT (MSH6)	XP_011531100.1:p.Lys173LeufsTer15
XM_011532799.1:c.401_402insACTGTTTT (MSH6)	XP_011531101.1:p.Lys135LeufsTer15
XM_011532800.1:c.401_402insACTGTTTT (MSH6)	XP_011531102.1:p.Lys135LeufsTer15
XM_024452819.1:c.698_699insACTGTTTT (MSH6)	XP_024308587.1:p.Lys234LeufsTer15
XM_024452820.1:c.515_516insACTGTTTT (MSH6)	XP_024308588.1:p.Lys173LeufsTer15
XM_024452821.1:c.401_402insACTGTTTT (MSH6)	XP_024308589.1:p.Lys135LeufsTer15
XM_024452822.1:c.-209_-208insACTGTTTT (MSH6)	XP_024308590.1:n.-209_-208insACTGTTTT
NM_000179.3:c.698_699insACTGTTTT (MSH6) MANE Select	NP_000170.1:p.Lys234LeufsTer15
NM_001281492.2:c.308_309insACTGTTTT (MSH6)	NP_001268421.1:p.Lys104LeufsTer15
NM_001281493.2:c.-209_-208insACTGTTTT (MSH6)	NP_001268422.1:n.-209_-208insACTGTTTT
NM_001281494.2:c.-209_-208insACTGTTTT (MSH6)	NP_001268423.1:n.-209_-208insACTGTTTT