Canonical Allele Identifier: CA2586964946

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804962_47804963insTCA , CM000664.2:g.47804962_47804963insTCA	GRCh38
NC_000002.11:g.48032101_48032102insTCA , CM000664.1:g.48032101_48032102insTCA	GRCh37
NC_000002.10:g.47885605_47885606insTCA	NCBI36
NG_007111.1:g.26816_26817insTCA , LRG_219:g.26816_26817insTCA
NG_008397.1:g.105713_105714insTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3194_3195insTCA (MSH6)	ENSP00000406248.2:p.Val1065_Cys1066insGln
ENST00000420813.6:c.3194_3195insTCA (MSH6)	ENSP00000390382.2:p.Val1065_Cys1066insGln
ENST00000455383.6:c.3194_3195insTCA (MSH6)	ENSP00000397484.2:p.Val1065_Cys1066insGln
ENST00000700004.2:c.3173-656_3173-655insTCA (MSH6)	ENSP00000514752.2:n.3173-656_3173-655insTCA
ENST00000699999.1:n.3575_3576insTCA (MSH6)
ENST00000700000.1:c.1925_1926insTCA (MSH6)	ENSP00000514749.1:p.Val642_Cys643insGln
ENST00000700002.1:c.3497_3498insTCA (MSH6)	ENSP00000514750.1:p.Val1166_Cys1167insGln
ENST00000700003.1:c.946_947insTCA (MSH6)	ENSP00000514751.1:n.946_947insTCA
ENST00000700004.1:c.2330-656_2330-655insTCA (MSH6)	ENSP00000514752.1:n.2330-656_2330-655insTCA
ENST00000700005.1:n.2342_2343insTCA (MSH6)
ENST00000700006.1:n.3563_3564insTCA (MSH6)
ENST00000700007.1:n.1496_1497insTCA (MSH6)
ENST00000700008.1:n.1070_1071insTCA (MSH6)
ENST00000700009.1:n.1069_1070insTCA (MSH6)
ENST00000700010.1:n.900_901insTCA (MSH6)
ENST00000700011.1:n.2195_2196insTCA (MSH6)
ENST00000234420.11:c.3491_3492insTCA (MSH6) MANE Select	ENSP00000234420.5:p.Val1164_Cys1165insGln
ENST00000540021.6:c.3101_3102insTCA (MSH6)	ENSP00000446475.1:p.Val1034_Cys1035insGln
ENST00000652107.1:c.3194_3195insTCA (MSH6)	ENSP00000498629.1:p.Val1065_Cys1066insGln
ENST00000673637.1:c.3194_3195insTCA (MSH6)	ENSP00000501310.1:p.Val1065_Cys1066insGln
ENST00000234420.9:c.3491_3492insTCA (MSH6)	ENSP00000234420.4:p.Val1164_Cys1165insGln
ENST00000405808.5:c.169+3232_169+3233insTGA (FBXO11)	ENSP00000385127.1:n.169+3232_169+3233insTGA
ENST00000434234.5:c.*124+3031_*124+3032insTGA (FBXO11)	ENSP00000402692.1:n.*124+3031_*124+3032insTGA
ENST00000445503.5:c.*2838_*2839insTCA (MSH6)	ENSP00000405294.1:n.*2838_*2839insTCA
ENST00000538136.1:c.2585_2586insTCA (MSH6)	ENSP00000438580.1:p.Val862_Cys863insGln
ENST00000540021.5:c.3101_3102insTCA (MSH6)	ENSP00000446475.1:p.Val1034_Cys1035insGln
ENST00000614496.4:c.2585_2586insTCA (MSH6)	ENSP00000477844.1:p.Val862_Cys863insGln
ENST00000622629.4:c.395_396insTCA (MSH6)	ENSP00000482078.1:p.Val132_Cys133insGln
NM_000179.2:c.3491_3492insTCA , LRG_219t1:c.3491_3492insTCA (MSH6)	NP_000170.1:p.Val1164_Cys1165insGln
NM_001281492.1:c.3101_3102insTCA (MSH6)	NP_001268421.1:p.Val1034_Cys1035insGln
NM_001281493.1:c.2585_2586insTCA (MSH6)	NP_001268422.1:p.Val862_Cys863insGln
NM_001281494.1:c.2585_2586insTCA (MSH6)	NP_001268423.1:p.Val862_Cys863insGln
XM_005264271.1:c.3194_3195insTCA (MSH6)	XP_005264328.1:p.Val1065_Cys1066insGln
XM_011532798.1:c.3308_3309insTCA (MSH6)	XP_011531100.1:p.Val1103_Cys1104insGln
XM_011532799.1:c.3194_3195insTCA (MSH6)	XP_011531101.1:p.Val1065_Cys1066insGln
XM_011532800.1:c.3194_3195insTCA (MSH6)	XP_011531102.1:p.Val1065_Cys1066insGln
XM_024452819.1:c.3491_3492insTCA (MSH6)	XP_024308587.1:p.Val1164_Cys1165insGln
XM_024452820.1:c.3308_3309insTCA (MSH6)	XP_024308588.1:p.Val1103_Cys1104insGln
XM_024452821.1:c.3194_3195insTCA (MSH6)	XP_024308589.1:p.Val1065_Cys1066insGln
XM_024452822.1:c.2585_2586insTCA (MSH6)	XP_024308590.1:p.Val862_Cys863insGln
NM_000179.3:c.3491_3492insTCA (MSH6) MANE Select	NP_000170.1:p.Val1164_Cys1165insGln
NM_001281492.2:c.3101_3102insTCA (MSH6)	NP_001268421.1:p.Val1034_Cys1035insGln
NM_001281493.2:c.2585_2586insTCA (MSH6)	NP_001268422.1:p.Val862_Cys863insGln
NM_001281494.2:c.2585_2586insTCA (MSH6)	NP_001268423.1:p.Val862_Cys863insGln