Canonical Allele Identifier: CA2555305465

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798688_47798689insGTG , CM000664.2:g.47798688_47798689insGTG	GRCh38
NC_000002.11:g.48025827_48025828insGTG , CM000664.1:g.48025827_48025828insGTG	GRCh37
NC_000002.10:g.47879331_47879332insGTG	NCBI36
NG_007111.1:g.20542_20543insGTG , LRG_219:g.20542_20543insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.408_409insGTG (MSH6)	ENSP00000406248.2:p.Thr136_Gln137insVal
ENST00000420813.6:c.408_409insGTG (MSH6)	ENSP00000390382.2:p.Thr136_Gln137insVal
ENST00000455383.6:c.408_409insGTG (MSH6)	ENSP00000397484.2:p.Thr136_Gln137insVal
ENST00000700004.2:c.705_706insGTG (MSH6)	ENSP00000514752.2:p.Thr235_Gln236insVal
ENST00000699999.1:n.789_790insGTG (MSH6)
ENST00000700000.1:c.705_706insGTG (MSH6)	ENSP00000514749.1:p.Thr235_Gln236insVal
ENST00000700002.1:c.711_712insGTG (MSH6)	ENSP00000514750.1:p.Thr237_Gln238insVal
ENST00000700003.1:c.627+2625_627+2626insGTG (MSH6)	ENSP00000514751.1:n.627+2625_627+2626insGTG
ENST00000234420.11:c.705_706insGTG (MSH6) MANE Select	ENSP00000234420.5:p.Thr235_Gln236insVal
ENST00000540021.6:c.315_316insGTG (MSH6)	ENSP00000446475.1:p.Thr105_Gln106insVal
ENST00000652107.1:c.408_409insGTG (MSH6)	ENSP00000498629.1:p.Thr136_Gln137insVal
ENST00000673637.1:c.408_409insGTG (MSH6)	ENSP00000501310.1:p.Thr136_Gln137insVal
ENST00000673922.1:n.427_428insGTG (MSH6)
ENST00000234420.9:c.705_706insGTG (MSH6)	ENSP00000234420.4:p.Thr235_Gln236insVal
ENST00000405808.5:c.170-9249_170-9248insCAC (FBXO11)	ENSP00000385127.1:n.170-9249_170-9248insCAC
ENST00000411819.1:c.408_409insGTG (MSH6)	ENSP00000406248.1:p.Thr136_Gln137insVal
ENST00000434234.5:c.*125-9249_*125-9248insCAC (FBXO11)	ENSP00000402692.1:n.*125-9249_*125-9248insCAC
ENST00000445503.5:c.*52_*53insGTG (MSH6)	ENSP00000405294.1:n.*52_*53insGTG
ENST00000456246.1:c.*193_*194insGTG (MSH6)	ENSP00000410570.1:n.*193_*194insGTG
ENST00000538136.1:c.-202_-201insGTG (MSH6)	ENSP00000438580.1:n.-202_-201insGTG
ENST00000540021.5:c.315_316insGTG (MSH6)	ENSP00000446475.1:p.Thr105_Gln106insVal
ENST00000614496.4:c.-202_-201insGTG (MSH6)	ENSP00000477844.1:n.-202_-201insGTG
ENST00000616033.4:c.702_703insGTG (MSH6)	ENSP00000480261.1:p.Thr234_Gln235insVal
ENST00000622629.4:c.-2392_-2391insGTG (MSH6)	ENSP00000482078.1:n.-2392_-2391insGTG
NM_000179.2:c.705_706insGTG , LRG_219t1:c.705_706insGTG (MSH6)	NP_000170.1:p.Thr235_Gln236insVal
NM_001281492.1:c.315_316insGTG (MSH6)	NP_001268421.1:p.Thr105_Gln106insVal
NM_001281493.1:c.-202_-201insGTG (MSH6)	NP_001268422.1:n.-202_-201insGTG
NM_001281494.1:c.-202_-201insGTG (MSH6)	NP_001268423.1:n.-202_-201insGTG
XM_005264271.1:c.408_409insGTG (MSH6)	XP_005264328.1:p.Thr136_Gln137insVal
XM_011532798.1:c.522_523insGTG (MSH6)	XP_011531100.1:p.Thr174_Gln175insVal
XM_011532799.1:c.408_409insGTG (MSH6)	XP_011531101.1:p.Thr136_Gln137insVal
XM_011532800.1:c.408_409insGTG (MSH6)	XP_011531102.1:p.Thr136_Gln137insVal
XM_024452819.1:c.705_706insGTG (MSH6)	XP_024308587.1:p.Thr235_Gln236insVal
XM_024452820.1:c.522_523insGTG (MSH6)	XP_024308588.1:p.Thr174_Gln175insVal
XM_024452821.1:c.408_409insGTG (MSH6)	XP_024308589.1:p.Thr136_Gln137insVal
XM_024452822.1:c.-202_-201insGTG (MSH6)	XP_024308590.1:n.-202_-201insGTG
NM_000179.3:c.705_706insGTG (MSH6) MANE Select	NP_000170.1:p.Thr235_Gln236insVal
NM_001281492.2:c.315_316insGTG (MSH6)	NP_001268421.1:p.Thr105_Gln106insVal
NM_001281493.2:c.-202_-201insGTG (MSH6)	NP_001268422.1:n.-202_-201insGTG
NM_001281494.2:c.-202_-201insGTG (MSH6)	NP_001268423.1:n.-202_-201insGTG