Canonical Allele Identifier: CA46707885

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs267608080

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799278_47799279delinsGCA , CM000664.2:g.47799278_47799279delinsGCA	GRCh38
NC_000002.11:g.48026417_48026418delinsGCA , CM000664.1:g.48026417_48026418delinsGCA	GRCh37
NC_000002.10:g.47879921_47879922delinsGCA	NCBI36
NG_007111.1:g.21132_21133delinsGCA , LRG_219:g.21132_21133delinsGCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.998_999delinsGCA (MSH6)	ENSP00000406248.2:p.Phe333CysfsTer3
ENST00000420813.6:c.998_999delinsGCA (MSH6)	ENSP00000390382.2:p.Phe333CysfsTer3
ENST00000455383.6:c.998_999delinsGCA (MSH6)	ENSP00000397484.2:p.Phe333CysfsTer3
ENST00000700004.2:c.1295_1296delinsGCA (MSH6)	ENSP00000514752.2:p.Phe432CysfsTer3
ENST00000699999.1:n.1379_1380delinsGCA (MSH6)
ENST00000700000.1:c.1295_1296delinsGCA (MSH6)	ENSP00000514749.1:p.Phe432CysfsTer3
ENST00000700002.1:c.1301_1302delinsGCA (MSH6)	ENSP00000514750.1:p.Phe434CysfsTer3
ENST00000700003.1:c.627+3215_627+3216delinsGCA (MSH6)	ENSP00000514751.1:n.627+3215_627+3216deli...
ENST00000700004.1:c.452_453delinsGCA (MSH6)	ENSP00000514752.1:p.Phe151CysfsTer3
ENST00000234420.11:c.1295_1296delinsGCA (MSH6) MANE Select	ENSP00000234420.5:p.Phe432CysfsTer3
ENST00000540021.6:c.905_906delinsGCA (MSH6)	ENSP00000446475.1:p.Phe302CysfsTer3
ENST00000652107.1:c.998_999delinsGCA (MSH6)	ENSP00000498629.1:p.Phe333CysfsTer3
ENST00000673637.1:c.998_999delinsGCA (MSH6)	ENSP00000501310.1:p.Phe333CysfsTer3
ENST00000234420.9:c.1295_1296delinsGCA (MSH6)	ENSP00000234420.4:p.Phe432CysfsTer3
ENST00000405808.5:c.169+8916_169+8917delinsTGC (FBXO11)	ENSP00000385127.1:n.169+8916_169+8917deli...
ENST00000434234.5:c.*124+8715_*124+8716delinsTGC (FBXO11)	ENSP00000402692.1:n.*124+8715_*124+8716de...
ENST00000445503.5:c.*642_*643delinsGCA (MSH6)	ENSP00000405294.1:n.*642_*643delinsGCA
ENST00000538136.1:c.389_390delinsGCA (MSH6)	ENSP00000438580.1:p.Phe130CysfsTer3
ENST00000540021.5:c.905_906delinsGCA (MSH6)	ENSP00000446475.1:p.Phe302CysfsTer3
ENST00000614496.4:c.389_390delinsGCA (MSH6)	ENSP00000477844.1:p.Phe130CysfsTer3
ENST00000616033.4:c.1292_1293delinsGCA (MSH6)	ENSP00000480261.1:p.Phe431CysfsTer3
ENST00000622629.4:c.-1802_-1801delinsGCA (MSH6)	ENSP00000482078.1:n.-1802_-1801delinsGCA
NM_000179.2:c.1295_1296delinsGCA , LRG_219t1:c.1295_1296delinsGCA (MSH6)	NP_000170.1:p.Phe432CysfsTer3
NM_001281492.1:c.905_906delinsGCA (MSH6)	NP_001268421.1:p.Phe302CysfsTer3
NM_001281493.1:c.389_390delinsGCA (MSH6)	NP_001268422.1:p.Phe130CysfsTer3
NM_001281494.1:c.389_390delinsGCA (MSH6)	NP_001268423.1:p.Phe130CysfsTer3
XM_005264271.1:c.998_999delinsGCA (MSH6)	XP_005264328.1:p.Phe333CysfsTer3
XM_011532798.1:c.1112_1113delinsGCA (MSH6)	XP_011531100.1:p.Phe371CysfsTer3
XM_011532799.1:c.998_999delinsGCA (MSH6)	XP_011531101.1:p.Phe333CysfsTer3
XM_011532800.1:c.998_999delinsGCA (MSH6)	XP_011531102.1:p.Phe333CysfsTer3
XM_024452819.1:c.1295_1296delinsGCA (MSH6)	XP_024308587.1:p.Phe432CysfsTer3
XM_024452820.1:c.1112_1113delinsGCA (MSH6)	XP_024308588.1:p.Phe371CysfsTer3
XM_024452821.1:c.998_999delinsGCA (MSH6)	XP_024308589.1:p.Phe333CysfsTer3
XM_024452822.1:c.389_390delinsGCA (MSH6)	XP_024308590.1:p.Phe130CysfsTer3
NM_000179.3:c.1295_1296delinsGCA (MSH6) MANE Select	NP_000170.1:p.Phe432CysfsTer3
NM_001281492.2:c.905_906delinsGCA (MSH6)	NP_001268421.1:p.Phe302CysfsTer3
NM_001281493.2:c.389_390delinsGCA (MSH6)	NP_001268422.1:p.Phe130CysfsTer3
NM_001281494.2:c.389_390delinsGCA (MSH6)	NP_001268423.1:p.Phe130CysfsTer3