Canonical Allele Identifier: CA2576961637

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806801_47806807del , CM000664.2:g.47806801_47806807del	GRCh38
NC_000002.11:g.48033940_48033946del , CM000664.1:g.48033940_48033946del	GRCh37
NC_000002.10:g.47887444_47887450del	NCBI36
NG_007111.1:g.28655_28661del , LRG_219:g.28655_28661del
NG_008397.1:g.103871_103877del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3727_3733del (MSH6)	ENSP00000406248.2:p.Arg1243LeufsTer2
ENST00000420813.6:c.3727_3733del (MSH6)	ENSP00000390382.2:p.Arg1243LeufsTer2
ENST00000455383.6:c.3727_3733del (MSH6)	ENSP00000397484.2:p.Arg1243LeufsTer2
ENST00000700004.2:c.3640_3646del (MSH6)	ENSP00000514752.2:p.Arg1214LeufsTer2
ENST00000699999.1:n.4698_4704del (MSH6)
ENST00000700000.1:c.2458_2464del (MSH6)	ENSP00000514749.1:p.Arg820LeufsTer2
ENST00000700002.1:c.4030_4036del (MSH6)	ENSP00000514750.1:p.Arg1344LeufsTer2
ENST00000700003.1:c.1479_1485del (MSH6)	ENSP00000514751.1:n.1479_1485del
ENST00000700004.1:c.2797_2803del (MSH6)	ENSP00000514752.1:p.Arg933LeufsTer2
ENST00000700005.1:n.3002_3008del (MSH6)
ENST00000700007.1:n.2619_2625del (MSH6)
ENST00000700008.1:n.2286_2292del (MSH6)
ENST00000700009.1:n.2688_2694del (MSH6)
ENST00000700010.1:n.1433_1439del (MSH6)
ENST00000700011.1:n.3318_3324del (MSH6)
ENST00000682451.1:n.3943_3949del (FBXO11)
ENST00000684712.1:n.4205_4211del (FBXO11)
ENST00000234420.11:c.4024_4030del (MSH6) MANE Select	ENSP00000234420.5:p.Arg1342LeufsTer2
ENST00000540021.6:c.3634_3640del (MSH6)	ENSP00000446475.1:p.Arg1212LeufsTer2
ENST00000652107.1:c.3727_3733del (MSH6)	ENSP00000498629.1:p.Arg1243LeufsTer2
ENST00000673637.1:c.3727_3733del (MSH6)	ENSP00000501310.1:p.Arg1243LeufsTer2
ENST00000234420.9:c.4024_4030del (MSH6)	ENSP00000234420.4:p.Arg1342LeufsTer2
ENST00000405808.5:c.169+1390_169+1396del (FBXO11)	ENSP00000385127.1:n.169+1390_169+1396del
ENST00000434234.5:c.*124+1189_*124+1195del (FBXO11)	ENSP00000402692.1:n.*124+1189_*124+1195del
ENST00000445503.5:c.*3371_*3377del (MSH6)	ENSP00000405294.1:n.*3371_*3377del
ENST00000465204.5:n.3105_3111del (FBXO11)
ENST00000538136.1:c.3118_3124del (MSH6)	ENSP00000438580.1:p.Arg1040LeufsTer2
ENST00000540021.5:c.3634_3640del (MSH6)	ENSP00000446475.1:p.Arg1212LeufsTer2
ENST00000614496.4:c.3118_3124del (MSH6)	ENSP00000477844.1:p.Arg1040LeufsTer2
ENST00000622629.4:c.925_931del (MSH6)	ENSP00000482078.1:p.Arg309LeufsTer2
NM_000179.2:c.4024_4030del , LRG_219t1:c.4024_4030del (MSH6)	NP_000170.1:p.Arg1342LeufsTer2
NM_001281492.1:c.3634_3640del (MSH6)	NP_001268421.1:p.Arg1212LeufsTer2
NM_001281493.1:c.3118_3124del (MSH6)	NP_001268422.1:p.Arg1040LeufsTer2
NM_001281494.1:c.3118_3124del (MSH6)	NP_001268423.1:p.Arg1040LeufsTer2
XM_005264271.1:c.3727_3733del (MSH6)	XP_005264328.1:p.Arg1243LeufsTer2
XM_011532798.1:c.3841_3847del (MSH6)	XP_011531100.1:p.Arg1281LeufsTer2
XM_011532799.1:c.3727_3733del (MSH6)	XP_011531101.1:p.Arg1243LeufsTer2
XM_011532800.1:c.3727_3733del (MSH6)	XP_011531102.1:p.Arg1243LeufsTer2
XM_024452819.1:c.4117_4123del (MSH6)	XP_024308587.1:p.Arg1373LeufsTer2
XM_024452820.1:c.3934_3940del (MSH6)	XP_024308588.1:p.Arg1312LeufsTer2
XM_024452821.1:c.3820_3826del (MSH6)	XP_024308589.1:p.Arg1274LeufsTer2
XM_024452822.1:c.3211_3217del (MSH6)	XP_024308590.1:p.Arg1071LeufsTer2
NM_000179.3:c.4024_4030del (MSH6) MANE Select	NP_000170.1:p.Arg1342LeufsTer2
NM_001281492.2:c.3634_3640del (MSH6)	NP_001268421.1:p.Arg1212LeufsTer2
NM_001281493.2:c.3118_3124del (MSH6)	NP_001268422.1:p.Arg1040LeufsTer2
NM_001281494.2:c.3118_3124del (MSH6)	NP_001268423.1:p.Arg1040LeufsTer2