Canonical Allele Identifier: CA2749798724

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798957_47798958insCACCCAACAC , CM000664.2:g.47798957_47798958insCACCCAACAC	GRCh38
NC_000002.11:g.48026096_48026097insCACCCAACAC , CM000664.1:g.48026096_48026097insCACCCAACAC	GRCh37
NC_000002.10:g.47879600_47879601insCACCCAACAC	NCBI36
NG_007111.1:g.20811_20812insCACCCAACAC , LRG_219:g.20811_20812insCACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.677_678insCACCCAACAC (MSH6)	ENSP00000406248.2:p.Gln226HisfsTer7
ENST00000420813.6:c.677_678insCACCCAACAC (MSH6)	ENSP00000390382.2:p.Gln226HisfsTer7
ENST00000455383.6:c.677_678insCACCCAACAC (MSH6)	ENSP00000397484.2:p.Gln226HisfsTer7
ENST00000700004.2:c.974_975insCACCCAACAC (MSH6)	ENSP00000514752.2:p.Gln325HisfsTer7
ENST00000699999.1:n.1058_1059insCACCCAACAC (MSH6)
ENST00000700000.1:c.974_975insCACCCAACAC (MSH6)	ENSP00000514749.1:p.Gln325HisfsTer7
ENST00000700002.1:c.980_981insCACCCAACAC (MSH6)	ENSP00000514750.1:p.Gln327HisfsTer7
ENST00000700003.1:c.627+2894_627+2895insCACCCAACAC (MSH6)	ENSP00000514751.1:n.627+2894_627+2895insCACCCAACAC
ENST00000700004.1:c.131_132insCACCCAACAC (MSH6)	ENSP00000514752.1:p.Gln44HisfsTer7
ENST00000234420.11:c.974_975insCACCCAACAC (MSH6) MANE Select	ENSP00000234420.5:p.Gln325HisfsTer7
ENST00000540021.6:c.584_585insCACCCAACAC (MSH6)	ENSP00000446475.1:p.Gln195HisfsTer7
ENST00000652107.1:c.677_678insCACCCAACAC (MSH6)	ENSP00000498629.1:p.Gln226HisfsTer7
ENST00000673637.1:c.677_678insCACCCAACAC (MSH6)	ENSP00000501310.1:p.Gln226HisfsTer7
ENST00000234420.9:c.974_975insCACCCAACAC (MSH6)	ENSP00000234420.4:p.Gln325HisfsTer7
ENST00000405808.5:c.169+9237_169+9238insGTGTTGGGTG (FBXO11)	ENSP00000385127.1:n.169+9237_169+9238insGTGTTGGGTG
ENST00000434234.5:c.*124+9036_*124+9037insGTGTTGGGTG (FBXO11)	ENSP00000402692.1:n.*124+9036_*124+9037insGTGTTGGGTG
ENST00000445503.5:c.*321_*322insCACCCAACAC (MSH6)	ENSP00000405294.1:n.*321_*322insCACCCAACAC
ENST00000538136.1:c.68_69insCACCCAACAC (MSH6)	ENSP00000438580.1:p.Gln23HisfsTer7
ENST00000540021.5:c.584_585insCACCCAACAC (MSH6)	ENSP00000446475.1:p.Gln195HisfsTer7
ENST00000614496.4:c.68_69insCACCCAACAC (MSH6)	ENSP00000477844.1:p.Gln23HisfsTer7
ENST00000616033.4:c.971_972insCACCCAACAC (MSH6)	ENSP00000480261.1:p.Gln324HisfsTer7
ENST00000622629.4:c.-2123_-2122insCACCCAACAC (MSH6)	ENSP00000482078.1:n.-2123_-2122insCACCCAACAC
NM_000179.2:c.974_975insCACCCAACAC , LRG_219t1:c.974_975insCACCCAACAC (MSH6)	NP_000170.1:p.Gln325HisfsTer7
NM_001281492.1:c.584_585insCACCCAACAC (MSH6)	NP_001268421.1:p.Gln195HisfsTer7
NM_001281493.1:c.68_69insCACCCAACAC (MSH6)	NP_001268422.1:p.Gln23HisfsTer7
NM_001281494.1:c.68_69insCACCCAACAC (MSH6)	NP_001268423.1:p.Gln23HisfsTer7
XM_005264271.1:c.677_678insCACCCAACAC (MSH6)	XP_005264328.1:p.Gln226HisfsTer7
XM_011532798.1:c.791_792insCACCCAACAC (MSH6)	XP_011531100.1:p.Gln264HisfsTer7
XM_011532799.1:c.677_678insCACCCAACAC (MSH6)	XP_011531101.1:p.Gln226HisfsTer7
XM_011532800.1:c.677_678insCACCCAACAC (MSH6)	XP_011531102.1:p.Gln226HisfsTer7
XM_024452819.1:c.974_975insCACCCAACAC (MSH6)	XP_024308587.1:p.Gln325HisfsTer7
XM_024452820.1:c.791_792insCACCCAACAC (MSH6)	XP_024308588.1:p.Gln264HisfsTer7
XM_024452821.1:c.677_678insCACCCAACAC (MSH6)	XP_024308589.1:p.Gln226HisfsTer7
XM_024452822.1:c.68_69insCACCCAACAC (MSH6)	XP_024308590.1:p.Gln23HisfsTer7
NM_000179.3:c.974_975insCACCCAACAC (MSH6) MANE Select	NP_000170.1:p.Gln325HisfsTer7
NM_001281492.2:c.584_585insCACCCAACAC (MSH6)	NP_001268421.1:p.Gln195HisfsTer7
NM_001281493.2:c.68_69insCACCCAACAC (MSH6)	NP_001268422.1:p.Gln23HisfsTer7
NM_001281494.2:c.68_69insCACCCAACAC (MSH6)	NP_001268423.1:p.Gln23HisfsTer7