Canonical Allele Identifier: CA2496048073

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798682_47798689delinsTAAGACAC , CM000664.2:g.47798682_47798689delinsTAAGACAC	GRCh38
NC_000002.11:g.48025821_48025828delinsTAAGACAC , CM000664.1:g.48025821_48025828delinsTAAGACAC	GRCh37
NC_000002.10:g.47879325_47879332delinsTAAGACAC	NCBI36
NG_007111.1:g.20536_20543delinsTAAGACAC , LRG_219:g.20536_20543delinsTAAGACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.402_409delinsTAAGACAC (MSH6)	ENSP00000406248.2:p.Pro134=
ENST00000420813.6:c.402_409delinsTAAGACAC (MSH6)	ENSP00000390382.2:p.Pro134=
ENST00000455383.6:c.402_409delinsTAAGACAC (MSH6)	ENSP00000397484.2:p.Pro134=
ENST00000700004.2:c.699_706delinsTAAGACAC (MSH6)	ENSP00000514752.2:p.Pro233=
ENST00000699999.1:n.783_790delinsTAAGACAC (MSH6)
ENST00000700000.1:c.699_706delinsTAAGACAC (MSH6)	ENSP00000514749.1:p.Pro233=
ENST00000700002.1:c.705_712delinsTAAGACAC (MSH6)	ENSP00000514750.1:p.Pro235=
ENST00000700003.1:c.627+2619_627+2626delinsTAAGACAC (MSH6)	ENSP00000514751.1:n.627+2619_627+2626delinsTAAGACAC
ENST00000234420.11:c.699_706delinsTAAGACAC (MSH6) MANE Select	ENSP00000234420.5:p.Pro233=
ENST00000540021.6:c.309_316delinsTAAGACAC (MSH6)	ENSP00000446475.1:p.Pro103=
ENST00000652107.1:c.402_409delinsTAAGACAC (MSH6)	ENSP00000498629.1:p.Pro134=
ENST00000673637.1:c.402_409delinsTAAGACAC (MSH6)	ENSP00000501310.1:p.Pro134=
ENST00000673922.1:n.421_428delinsTAAGACAC (MSH6)
ENST00000234420.9:c.699_706delinsTAAGACAC (MSH6)	ENSP00000234420.4:p.Pro233=
ENST00000405808.5:c.170-9249_170-9242delinsGTGTCTTA (FBXO11)	ENSP00000385127.1:n.170-9249_170-9242delinsGTGTCTTA
ENST00000411819.1:c.402_409delinsTAAGACAC (MSH6)	ENSP00000406248.1:p.Pro134=
ENST00000434234.5:c.*125-9249_*125-9242delinsGTGTCTTA (FBXO11)	ENSP00000402692.1:n.*125-9249_*125-9242delinsGTGTCTTA
ENST00000445503.5:c.*46_*53delinsTAAGACAC (MSH6)	ENSP00000405294.1:n.*46_*53delinsTAAGACAC
ENST00000456246.1:c.*187_*194delinsTAAGACAC (MSH6)	ENSP00000410570.1:n.*187_*194delinsTAAGACAC
ENST00000538136.1:c.-208_-201delinsTAAGACAC (MSH6)	ENSP00000438580.1:n.-208_-201delinsTAAGACAC
ENST00000540021.5:c.309_316delinsTAAGACAC (MSH6)	ENSP00000446475.1:p.Pro103=
ENST00000614496.4:c.-208_-201delinsTAAGACAC (MSH6)	ENSP00000477844.1:n.-208_-201delinsTAAGACAC
ENST00000616033.4:c.696_703delinsTAAGACAC (MSH6)	ENSP00000480261.1:p.Pro232=
ENST00000622629.4:c.-2398_-2391delinsTAAGACAC (MSH6)	ENSP00000482078.1:n.-2398_-2391delinsTAAGACAC
NM_000179.2:c.699_706delinsTAAGACAC , LRG_219t1:c.699_706delinsTAAGACAC (MSH6)	NP_000170.1:p.Pro233=
NM_001281492.1:c.309_316delinsTAAGACAC (MSH6)	NP_001268421.1:p.Pro103=
NM_001281493.1:c.-208_-201delinsTAAGACAC (MSH6)	NP_001268422.1:n.-208_-201delinsTAAGACAC
NM_001281494.1:c.-208_-201delinsTAAGACAC (MSH6)	NP_001268423.1:n.-208_-201delinsTAAGACAC
XM_005264271.1:c.402_409delinsTAAGACAC (MSH6)	XP_005264328.1:p.Pro134=
XM_011532798.1:c.516_523delinsTAAGACAC (MSH6)	XP_011531100.1:p.Pro172=
XM_011532799.1:c.402_409delinsTAAGACAC (MSH6)	XP_011531101.1:p.Pro134=
XM_011532800.1:c.402_409delinsTAAGACAC (MSH6)	XP_011531102.1:p.Pro134=
XM_024452819.1:c.699_706delinsTAAGACAC (MSH6)	XP_024308587.1:p.Pro233=
XM_024452820.1:c.516_523delinsTAAGACAC (MSH6)	XP_024308588.1:p.Pro172=
XM_024452821.1:c.402_409delinsTAAGACAC (MSH6)	XP_024308589.1:p.Pro134=
XM_024452822.1:c.-208_-201delinsTAAGACAC (MSH6)	XP_024308590.1:n.-208_-201delinsTAAGACAC
NM_000179.3:c.699_706delinsTAAGACAC (MSH6) MANE Select	NP_000170.1:p.Pro233=
NM_001281492.2:c.309_316delinsTAAGACAC (MSH6)	NP_001268421.1:p.Pro103=
NM_001281493.2:c.-208_-201delinsTAAGACAC (MSH6)	NP_001268422.1:n.-208_-201delinsTAAGACAC
NM_001281494.2:c.-208_-201delinsTAAGACAC (MSH6)	NP_001268423.1:n.-208_-201delinsTAAGACAC