Canonical Allele Identifier: CA2838032284

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806611dup , CM000664.2:g.47806611dup	GRCh38
NC_000002.11:g.48033750dup , CM000664.1:g.48033750dup	GRCh37
NC_000002.10:g.47887254dup	NCBI36
NG_007111.1:g.28465dup , LRG_219:g.28465dup
NG_008397.1:g.104066dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3664dup (MSH6)	ENSP00000406248.2:p.Arg1222LysfsTer4
ENST00000420813.6:c.3664dup (MSH6)	ENSP00000390382.2:p.Arg1222LysfsTer4
ENST00000455383.6:c.3664dup (MSH6)	ENSP00000397484.2:p.Arg1222LysfsTer4
ENST00000700004.2:c.3577dup (MSH6)	ENSP00000514752.2:p.Arg1193LysfsTer4
ENST00000699999.1:n.4635dup (MSH6)
ENST00000700000.1:c.2395dup (MSH6)	ENSP00000514749.1:p.Arg799LysfsTer4
ENST00000700002.1:c.3967dup (MSH6)	ENSP00000514750.1:p.Arg1323LysfsTer4
ENST00000700003.1:c.1416dup (MSH6)	ENSP00000514751.1:n.1416dup
ENST00000700004.1:c.2734dup (MSH6)	ENSP00000514752.1:p.Arg912LysfsTer4
ENST00000700005.1:n.2812dup (MSH6)
ENST00000700006.1:n.5119dup (MSH6)
ENST00000700007.1:n.2556dup (MSH6)
ENST00000700008.1:n.2223dup (MSH6)
ENST00000700009.1:n.2625dup (MSH6)
ENST00000700010.1:n.1370dup (MSH6)
ENST00000700011.1:n.3255dup (MSH6)
ENST00000682451.1:n.4138dup (FBXO11)
ENST00000684712.1:n.4400dup (FBXO11)
ENST00000234420.11:c.3961dup (MSH6) MANE Select	ENSP00000234420.5:p.Arg1321LysfsTer4
ENST00000540021.6:c.3571dup (MSH6)	ENSP00000446475.1:p.Arg1191LysfsTer4
ENST00000652107.1:c.3664dup (MSH6)	ENSP00000498629.1:p.Arg1222LysfsTer4
ENST00000673637.1:c.3664dup (MSH6)	ENSP00000501310.1:p.Arg1222LysfsTer4
ENST00000234420.9:c.3961dup (MSH6)	ENSP00000234420.4:p.Arg1321LysfsTer4
ENST00000405808.5:c.169+1585dup (FBXO11)	ENSP00000385127.1:n.169+1585dup
ENST00000434234.5:c.*124+1384dup (FBXO11)	ENSP00000402692.1:n.*124+1384dup
ENST00000445503.5:c.*3308dup (MSH6)	ENSP00000405294.1:n.*3308dup
ENST00000538136.1:c.3055dup (MSH6)	ENSP00000438580.1:p.Arg1019LysfsTer4
ENST00000540021.5:c.3571dup (MSH6)	ENSP00000446475.1:p.Arg1191LysfsTer4
ENST00000614496.4:c.3055dup (MSH6)	ENSP00000477844.1:p.Arg1019LysfsTer4
ENST00000622629.4:c.862dup (MSH6)	ENSP00000482078.1:p.Arg288LysfsTer4
NM_000179.2:c.3961dup , LRG_219t1:c.3961dup (MSH6)	NP_000170.1:p.Arg1321LysfsTer4
NM_001281492.1:c.3571dup (MSH6)	NP_001268421.1:p.Arg1191LysfsTer4
NM_001281493.1:c.3055dup (MSH6)	NP_001268422.1:p.Arg1019LysfsTer4
NM_001281494.1:c.3055dup (MSH6)	NP_001268423.1:p.Arg1019LysfsTer4
XM_005264271.1:c.3664dup (MSH6)	XP_005264328.1:p.Arg1222LysfsTer4
XM_011532798.1:c.3778dup (MSH6)	XP_011531100.1:p.Arg1260LysfsTer4
XM_011532799.1:c.3664dup (MSH6)	XP_011531101.1:p.Arg1222LysfsTer4
XM_011532800.1:c.3664dup (MSH6)	XP_011531102.1:p.Arg1222LysfsTer4
XM_024452819.1:c.4054dup (MSH6)	XP_024308587.1:p.Arg1352LysfsTer4
XM_024452820.1:c.3871dup (MSH6)	XP_024308588.1:p.Arg1291LysfsTer4
XM_024452821.1:c.3757dup (MSH6)	XP_024308589.1:p.Arg1253LysfsTer4
XM_024452822.1:c.3148dup (MSH6)	XP_024308590.1:p.Arg1050LysfsTer4
NM_000179.3:c.3961dup (MSH6) MANE Select	NP_000170.1:p.Arg1321LysfsTer4
NM_001281492.2:c.3571dup (MSH6)	NP_001268421.1:p.Arg1191LysfsTer4
NM_001281493.2:c.3055dup (MSH6)	NP_001268422.1:p.Arg1019LysfsTer4
NM_001281494.2:c.3055dup (MSH6)	NP_001268423.1:p.Arg1019LysfsTer4