Canonical Allele Identifier: CA426122191

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806613A>G , CM000664.2:g.47806613A>G	GRCh38
NC_000002.11:g.48033752A>G , CM000664.1:g.48033752A>G	GRCh37
NC_000002.10:g.47887256A>G	NCBI36
NG_007111.1:g.28467A>G , LRG_219:g.28467A>G
NG_008397.1:g.104063T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000179.3:c.3963A>G (MSH6) MANE Select	NP_000170.1:p.Arg1321=
ENST00000234420.11:c.3963A>G (MSH6) MANE Select	ENSP00000234420.5:p.Arg1321=
NM_000179.2:c.3963A>G , LRG_219t1:c.3963A>G (MSH6)	NP_000170.1:p.Arg1321=
NM_001281492.1:c.3573A>G (MSH6)	NP_001268421.1:p.Arg1191=
NM_001281492.2:c.3573A>G (MSH6)	NP_001268421.1:p.Arg1191=
NM_001281493.1:c.3057A>G (MSH6)	NP_001268422.1:p.Arg1019=
NM_001281493.2:c.3057A>G (MSH6)	NP_001268422.1:p.Arg1019=
NM_001281494.1:c.3057A>G (MSH6)	NP_001268423.1:p.Arg1019=
NM_001281494.2:c.3057A>G (MSH6)	NP_001268423.1:p.Arg1019=
ENST00000234420.9:c.3963A>G (MSH6)	ENSP00000234420.4:p.Arg1321=
ENST00000405808.5:c.169+1582T>C (FBXO11)	ENSP00000385127.1:n.169+1582T>C
ENST00000411819.2:c.3666A>G (MSH6)	ENSP00000406248.2:p.Arg1222=
ENST00000420813.6:c.3666A>G (MSH6)	ENSP00000390382.2:p.Arg1222=
ENST00000434234.5:c.*124+1381T>C (FBXO11)	ENSP00000402692.1:n.*124+1381T>C
ENST00000445503.5:c.*3310A>G (MSH6)	ENSP00000405294.1:n.*3310A>G
ENST00000455383.6:c.3666A>G (MSH6)	ENSP00000397484.2:p.Arg1222=
ENST00000538136.1:c.3057A>G (MSH6)	ENSP00000438580.1:p.Arg1019=
ENST00000540021.5:c.3573A>G (MSH6)	ENSP00000446475.1:p.Arg1191=
ENST00000540021.6:c.3573A>G (MSH6)	ENSP00000446475.1:p.Arg1191=
ENST00000614496.4:c.3057A>G (MSH6)	ENSP00000477844.1:p.Arg1019=
ENST00000622629.4:c.864A>G (MSH6)	ENSP00000482078.1:p.Arg288=
ENST00000652107.1:c.3666A>G (MSH6)	ENSP00000498629.1:p.Arg1222=
ENST00000673637.1:c.3666A>G (MSH6)	ENSP00000501310.1:p.Arg1222=
ENST00000682451.1:n.4135T>C (FBXO11)
ENST00000684712.1:n.4397T>C (FBXO11)
ENST00000699999.1:n.4637A>G (MSH6)
ENST00000700000.1:c.2397A>G (MSH6)	ENSP00000514749.1:p.Arg799=
ENST00000700002.1:c.3969A>G (MSH6)	ENSP00000514750.1:p.Arg1323=
ENST00000700003.1:c.1418A>G (MSH6)	ENSP00000514751.1:n.1418A>G
ENST00000700004.1:c.2736A>G (MSH6)	ENSP00000514752.1:p.Arg912=
ENST00000700004.2:c.3579A>G (MSH6)	ENSP00000514752.2:p.Arg1193=
ENST00000700005.1:n.2814A>G (MSH6)
ENST00000700006.1:n.5121A>G (MSH6)
ENST00000700007.1:n.2558A>G (MSH6)
ENST00000700008.1:n.2225A>G (MSH6)
ENST00000700009.1:n.2627A>G (MSH6)
ENST00000700010.1:n.1372A>G (MSH6)
ENST00000700011.1:n.3257A>G (MSH6)
XM_005264271.1:c.3666A>G (MSH6)	XP_005264328.1:p.Arg1222=
XM_011532798.1:c.3780A>G (MSH6)	XP_011531100.1:p.Arg1260=
XM_011532799.1:c.3666A>G (MSH6)	XP_011531101.1:p.Arg1222=
XM_011532800.1:c.3666A>G (MSH6)	XP_011531102.1:p.Arg1222=
XM_024452819.1:c.4056A>G (MSH6)	XP_024308587.1:p.Arg1352=
XM_024452820.1:c.3873A>G (MSH6)	XP_024308588.1:p.Arg1291=
XM_024452821.1:c.3759A>G (MSH6)	XP_024308589.1:p.Arg1253=
XM_024452822.1:c.3150A>G (MSH6)	XP_024308590.1:p.Arg1050=