Canonical Allele Identifier: CA2496054389

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806664_47806675delinsCTATAATGGAAT , CM000664.2:g.47806664_47806675delinsCTATAATGGAAT	GRCh38
NC_000002.11:g.48033803_48033814delinsCTATAATGGAAT , CM000664.1:g.48033803_48033814delinsCTATAATGGAAT	GRCh37
NC_000002.10:g.47887307_47887318delinsCTATAATGGAAT	NCBI36
NG_007111.1:g.28518_28529delinsCTATAATGGAAT , LRG_219:g.28518_28529delinsCTATAATGGAAT
NG_008397.1:g.104001_104012delinsATTCCATTATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	ENSP00000406248.2:n.3704+13_3704+24delinsCTATAATGGAAT
ENST00000420813.6:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	ENSP00000390382.2:n.3704+13_3704+24delinsCTATAATGGAAT
ENST00000455383.6:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	ENSP00000397484.2:n.3704+13_3704+24delinsCTATAATGGAAT
ENST00000700004.2:c.3617+13_3617+24delinsCTATAATGGAAT (MSH6)	ENSP00000514752.2:n.3617+13_3617+24delinsCTATAATGGAAT
ENST00000699999.1:n.4675+13_4675+24delinsCTATAATGGAAT (MSH6)
ENST00000700000.1:c.2435+13_2435+24delinsCTATAATGGAAT (MSH6)	ENSP00000514749.1:n.2435+13_2435+24delinsCTATAATGGAAT
ENST00000700002.1:c.4007+13_4007+24delinsCTATAATGGAAT (MSH6)	ENSP00000514750.1:n.4007+13_4007+24delinsCTATAATGGAAT
ENST00000700003.1:c.1456+13_1456+24delinsCTATAATGGAAT (MSH6)	ENSP00000514751.1:n.1456+13_1456+24delinsCTATAATGGAAT
ENST00000700004.1:c.2774+13_2774+24delinsCTATAATGGAAT (MSH6)	ENSP00000514752.1:n.2774+13_2774+24delinsCTATAATGGAAT
ENST00000700005.1:n.2865_2876delinsCTATAATGGAAT (MSH6)
ENST00000700006.1:n.5172_5183delinsCTATAATGGAAT (MSH6)
ENST00000700007.1:n.2596+13_2596+24delinsCTATAATGGAAT (MSH6)
ENST00000700008.1:n.2263+13_2263+24delinsCTATAATGGAAT (MSH6)
ENST00000700009.1:n.2665+13_2665+24delinsCTATAATGGAAT (MSH6)
ENST00000700010.1:n.1410+13_1410+24delinsCTATAATGGAAT (MSH6)
ENST00000700011.1:n.3295+13_3295+24delinsCTATAATGGAAT (MSH6)
ENST00000682451.1:n.4073_4084delinsATTCCATTATAG (FBXO11)
ENST00000684712.1:n.4335_4346delinsATTCCATTATAG (FBXO11)
ENST00000234420.11:c.4001+13_4001+24delinsCTATAATGGAAT (MSH6) MANE Select	ENSP00000234420.5:n.4001+13_4001+24delinsCTATAATGGAAT
ENST00000540021.6:c.3611+13_3611+24delinsCTATAATGGAAT (MSH6)	ENSP00000446475.1:n.3611+13_3611+24delinsCTATAATGGAAT
ENST00000652107.1:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	ENSP00000498629.1:n.3704+13_3704+24delinsCTATAATGGAAT
ENST00000673637.1:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	ENSP00000501310.1:n.3704+13_3704+24delinsCTATAATGGAAT
ENST00000234420.9:c.4001+13_4001+24delinsCTATAATGGAAT (MSH6)	ENSP00000234420.4:n.4001+13_4001+24delinsCTATAATGGAAT
ENST00000405808.5:c.169+1520_169+1531delinsATTCCATTATAG (FBXO11)	ENSP00000385127.1:n.169+1520_169+1531delinsATTCCATTATAG
ENST00000434234.5:c.*124+1319_*124+1330delinsATTCCATTATAG (FBXO11)	ENSP00000402692.1:n.*124+1319_*124+1330delinsATTCCATTATAG
ENST00000445503.5:c.*3348+13_*3348+24delinsCTATAATGGAAT (MSH6)	ENSP00000405294.1:n.*3348+13_*3348+24delinsCTATAATGGAAT
ENST00000538136.1:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	ENSP00000438580.1:n.3095+13_3095+24delinsCTATAATGGAAT
ENST00000540021.5:c.3611+13_3611+24delinsCTATAATGGAAT (MSH6)	ENSP00000446475.1:n.3611+13_3611+24delinsCTATAATGGAAT
ENST00000614496.4:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	ENSP00000477844.1:n.3095+13_3095+24delinsCTATAATGGAAT
ENST00000622629.4:c.902+13_902+24delinsCTATAATGGAAT (MSH6)	ENSP00000482078.1:n.902+13_902+24delinsCTATAATGGAAT
NM_000179.2:c.4001+13_4001+24delinsCTATAATGGAAT , LRG_219t1:c.4001+13_4001+24delinsCTATAATGGAAT (MSH6)	NP_000170.1:n.4001+13_4001+24delinsCTATAATGGAAT
NM_001281492.1:c.3611+13_3611+24delinsCTATAATGGAAT (MSH6)	NP_001268421.1:n.3611+13_3611+24delinsCTATAATGGAAT
NM_001281493.1:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	NP_001268422.1:n.3095+13_3095+24delinsCTATAATGGAAT
NM_001281494.1:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	NP_001268423.1:n.3095+13_3095+24delinsCTATAATGGAAT
XM_005264271.1:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	XP_005264328.1:n.3704+13_3704+24delinsCTATAATGGAAT
XM_011532798.1:c.3818+13_3818+24delinsCTATAATGGAAT (MSH6)	XP_011531100.1:n.3818+13_3818+24delinsCTATAATGGAAT
XM_011532799.1:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	XP_011531101.1:n.3704+13_3704+24delinsCTATAATGGAAT
XM_011532800.1:c.3704+13_3704+24delinsCTATAATGGAAT (MSH6)	XP_011531102.1:n.3704+13_3704+24delinsCTATAATGGAAT
XM_024452819.1:c.4094+13_4094+24delinsCTATAATGGAAT (MSH6)	XP_024308587.1:n.4094+13_4094+24delinsCTATAATGGAAT
XM_024452820.1:c.3911+13_3911+24delinsCTATAATGGAAT (MSH6)	XP_024308588.1:n.3911+13_3911+24delinsCTATAATGGAAT
XM_024452821.1:c.3797+13_3797+24delinsCTATAATGGAAT (MSH6)	XP_024308589.1:n.3797+13_3797+24delinsCTATAATGGAAT
XM_024452822.1:c.3188+13_3188+24delinsCTATAATGGAAT (MSH6)	XP_024308590.1:n.3188+13_3188+24delinsCTATAATGGAAT
NM_000179.3:c.4001+13_4001+24delinsCTATAATGGAAT (MSH6) MANE Select	NP_000170.1:n.4001+13_4001+24delinsCTATAATGGAAT
NM_001281492.2:c.3611+13_3611+24delinsCTATAATGGAAT (MSH6)	NP_001268421.1:n.3611+13_3611+24delinsCTATAATGGAAT
NM_001281493.2:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	NP_001268422.1:n.3095+13_3095+24delinsCTATAATGGAAT
NM_001281494.2:c.3095+13_3095+24delinsCTATAATGGAAT (MSH6)	NP_001268423.1:n.3095+13_3095+24delinsCTATAATGGAAT