Canonical Allele Identifier: CA2496053973

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806390_47806393delinsGGTT , CM000664.2:g.47806390_47806393delinsGGTT	GRCh38
NC_000002.11:g.48033529_48033532delinsGGTT , CM000664.1:g.48033529_48033532delinsGGTT	GRCh37
NC_000002.10:g.47887033_47887036delinsGGTT	NCBI36
NG_007111.1:g.28244_28247delinsGGTT , LRG_219:g.28244_28247delinsGGTT
NG_008397.1:g.104283_104286delinsAACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3504+32_3504+35delinsGGTT (MSH6)	ENSP00000406248.2:n.3504+32_3504+35delinsGGTT
ENST00000420813.6:c.3504+32_3504+35delinsGGTT (MSH6)	ENSP00000390382.2:n.3504+32_3504+35delinsGGTT
ENST00000455383.6:c.3504+32_3504+35delinsGGTT (MSH6)	ENSP00000397484.2:n.3504+32_3504+35delinsGGTT
ENST00000700004.2:c.3417+32_3417+35delinsGGTT (MSH6)	ENSP00000514752.2:n.3417+32_3417+35delinsGGTT
ENST00000699999.1:n.4475+32_4475+35delinsGGTT (MSH6)
ENST00000700000.1:c.2235+32_2235+35delinsGGTT (MSH6)	ENSP00000514749.1:n.2235+32_2235+35delinsGGTT
ENST00000700002.1:c.3807+32_3807+35delinsGGTT (MSH6)	ENSP00000514750.1:n.3807+32_3807+35delinsGGTT
ENST00000700003.1:c.1256+32_1256+35delinsGGTT (MSH6)	ENSP00000514751.1:n.1256+32_1256+35delinsGGTT
ENST00000700004.1:c.2574+32_2574+35delinsGGTT (MSH6)	ENSP00000514752.1:n.2574+32_2574+35delinsGGTT
ENST00000700005.1:n.2652+32_2652+35delinsGGTT (MSH6)
ENST00000700006.1:n.4959+32_4959+35delinsGGTT (MSH6)
ENST00000700007.1:n.2396+32_2396+35delinsGGTT (MSH6)
ENST00000700008.1:n.2002_2005delinsGGTT (MSH6)
ENST00000700009.1:n.2465+32_2465+35delinsGGTT (MSH6)
ENST00000700010.1:n.1210+32_1210+35delinsGGTT (MSH6)
ENST00000700011.1:n.3095+32_3095+35delinsGGTT (MSH6)
ENST00000682451.1:n.4355_4358delinsAACC (FBXO11)
ENST00000684712.1:n.4617_4620delinsAACC (FBXO11)
ENST00000234420.11:c.3801+32_3801+35delinsGGTT (MSH6) MANE Select	ENSP00000234420.5:n.3801+32_3801+35delinsGGTT
ENST00000540021.6:c.3411+32_3411+35delinsGGTT (MSH6)	ENSP00000446475.1:n.3411+32_3411+35delinsGGTT
ENST00000652107.1:c.3504+32_3504+35delinsGGTT (MSH6)	ENSP00000498629.1:n.3504+32_3504+35delinsGGTT
ENST00000673637.1:c.3504+32_3504+35delinsGGTT (MSH6)	ENSP00000501310.1:n.3504+32_3504+35delinsGGTT
ENST00000234420.9:c.3801+32_3801+35delinsGGTT (MSH6)	ENSP00000234420.4:n.3801+32_3801+35delinsGGTT
ENST00000405808.5:c.169+1802_169+1805delinsAACC (FBXO11)	ENSP00000385127.1:n.169+1802_169+1805delinsAACC
ENST00000434234.5:c.*124+1601_*124+1604delinsAACC (FBXO11)	ENSP00000402692.1:n.*124+1601_*124+1604delinsAACC
ENST00000445503.5:c.*3148+32_*3148+35delinsGGTT (MSH6)	ENSP00000405294.1:n.*3148+32_*3148+35delinsGGTT
ENST00000538136.1:c.2895+32_2895+35delinsGGTT (MSH6)	ENSP00000438580.1:n.2895+32_2895+35delinsGGTT
ENST00000540021.5:c.3411+32_3411+35delinsGGTT (MSH6)	ENSP00000446475.1:n.3411+32_3411+35delinsGGTT
ENST00000614496.4:c.2895+32_2895+35delinsGGTT (MSH6)	ENSP00000477844.1:n.2895+32_2895+35delinsGGTT
ENST00000622629.4:c.702+32_702+35delinsGGTT (MSH6)	ENSP00000482078.1:n.702+32_702+35delinsGGTT
NM_000179.2:c.3801+32_3801+35delinsGGTT , LRG_219t1:c.3801+32_3801+35delinsGGTT (MSH6)	NP_000170.1:n.3801+32_3801+35delinsGGTT
NM_001281492.1:c.3411+32_3411+35delinsGGTT (MSH6)	NP_001268421.1:n.3411+32_3411+35delinsGGTT
NM_001281493.1:c.2895+32_2895+35delinsGGTT (MSH6)	NP_001268422.1:n.2895+32_2895+35delinsGGTT
NM_001281494.1:c.2895+32_2895+35delinsGGTT (MSH6)	NP_001268423.1:n.2895+32_2895+35delinsGGTT
XM_005264271.1:c.3504+32_3504+35delinsGGTT (MSH6)	XP_005264328.1:n.3504+32_3504+35delinsGGTT
XM_011532798.1:c.3618+32_3618+35delinsGGTT (MSH6)	XP_011531100.1:n.3618+32_3618+35delinsGGTT
XM_011532799.1:c.3504+32_3504+35delinsGGTT (MSH6)	XP_011531101.1:n.3504+32_3504+35delinsGGTT
XM_011532800.1:c.3504+32_3504+35delinsGGTT (MSH6)	XP_011531102.1:n.3504+32_3504+35delinsGGTT
XM_024452819.1:c.3833_3836delinsGGTT (MSH6)	XP_024308587.1:p.Arg1278=
XM_024452820.1:c.3650_3653delinsGGTT (MSH6)	XP_024308588.1:p.Arg1217=
XM_024452821.1:c.3536_3539delinsGGTT (MSH6)	XP_024308589.1:p.Arg1179=
XM_024452822.1:c.2927_2930delinsGGTT (MSH6)	XP_024308590.1:p.Arg976=
NM_000179.3:c.3801+32_3801+35delinsGGTT (MSH6) MANE Select	NP_000170.1:n.3801+32_3801+35delinsGGTT
NM_001281492.2:c.3411+32_3411+35delinsGGTT (MSH6)	NP_001268421.1:n.3411+32_3411+35delinsGGTT
NM_001281493.2:c.2895+32_2895+35delinsGGTT (MSH6)	NP_001268422.1:n.2895+32_2895+35delinsGGTT
NM_001281494.2:c.2895+32_2895+35delinsGGTT (MSH6)	NP_001268423.1:n.2895+32_2895+35delinsGGTT