Canonical Allele Identifier: CA2496053488

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805648A= , CM000664.2:g.47805648A=	GRCh38
NC_000002.11:g.48032787A= , CM000664.1:g.48032787A=	GRCh37
NC_000002.10:g.47886291A=	NCBI36
NG_007111.1:g.27502A= , LRG_219:g.27502A=
NG_008397.1:g.105028T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3290A= (MSH6)	ENSP00000406248.2:p.Glu1097=
ENST00000420813.6:c.3290A= (MSH6)	ENSP00000390382.2:p.Glu1097=
ENST00000455383.6:c.3290A= (MSH6)	ENSP00000397484.2:p.Glu1097=
ENST00000700004.2:c.3203A= (MSH6)	ENSP00000514752.2:p.Glu1068=
ENST00000699999.1:n.4261A= (MSH6)
ENST00000700000.1:c.2021A= (MSH6)	ENSP00000514749.1:p.Glu674=
ENST00000700002.1:c.3593A= (MSH6)	ENSP00000514750.1:p.Glu1198=
ENST00000700003.1:c.1042A= (MSH6)	ENSP00000514751.1:n.1042A=
ENST00000700004.1:c.2360A= (MSH6)	ENSP00000514752.1:p.Glu787=
ENST00000700005.1:n.2438A= (MSH6)
ENST00000700006.1:n.4249A= (MSH6)
ENST00000700007.1:n.2182A= (MSH6)
ENST00000700008.1:n.1756A= (MSH6)
ENST00000700009.1:n.1755A= (MSH6)
ENST00000700010.1:n.996A= (MSH6)
ENST00000700011.1:n.2881A= (MSH6)
ENST00000234420.11:c.3587A= (MSH6) MANE Select	ENSP00000234420.5:p.Glu1196=
ENST00000540021.6:c.3197A= (MSH6)	ENSP00000446475.1:p.Glu1066=
ENST00000652107.1:c.3290A= (MSH6)	ENSP00000498629.1:p.Glu1097=
ENST00000673637.1:c.3290A= (MSH6)	ENSP00000501310.1:p.Glu1097=
ENST00000234420.9:c.3587A= (MSH6)	ENSP00000234420.4:p.Glu1196=
ENST00000405808.5:c.169+2547T= (FBXO11)	ENSP00000385127.1:n.169+2547T=
ENST00000434234.5:c.*124+2346T= (FBXO11)	ENSP00000402692.1:n.*124+2346T=
ENST00000445503.5:c.*2934A= (MSH6)	ENSP00000405294.1:n.*2934A=
ENST00000538136.1:c.2681A= (MSH6)	ENSP00000438580.1:p.Glu894=
ENST00000540021.5:c.3197A= (MSH6)	ENSP00000446475.1:p.Glu1066=
ENST00000614496.4:c.2681A= (MSH6)	ENSP00000477844.1:p.Glu894=
ENST00000622629.4:c.491A= (MSH6)	ENSP00000482078.1:p.Glu164=
NM_000179.2:c.3587A= , LRG_219t1:c.3587A= (MSH6)	NP_000170.1:p.Glu1196=
NM_001281492.1:c.3197A= (MSH6)	NP_001268421.1:p.Glu1066=
NM_001281493.1:c.2681A= (MSH6)	NP_001268422.1:p.Glu894=
NM_001281494.1:c.2681A= (MSH6)	NP_001268423.1:p.Glu894=
XM_005264271.1:c.3290A= (MSH6)	XP_005264328.1:p.Glu1097=
XM_011532798.1:c.3404A= (MSH6)	XP_011531100.1:p.Glu1135=
XM_011532799.1:c.3290A= (MSH6)	XP_011531101.1:p.Glu1097=
XM_011532800.1:c.3290A= (MSH6)	XP_011531102.1:p.Glu1097=
XM_024452819.1:c.3587A= (MSH6)	XP_024308587.1:p.Glu1196=
XM_024452820.1:c.3404A= (MSH6)	XP_024308588.1:p.Glu1135=
XM_024452821.1:c.3290A= (MSH6)	XP_024308589.1:p.Glu1097=
XM_024452822.1:c.2681A= (MSH6)	XP_024308590.1:p.Glu894=
NM_000179.3:c.3587A= (MSH6) MANE Select	NP_000170.1:p.Glu1196=
NM_001281492.2:c.3197A= (MSH6)	NP_001268421.1:p.Glu1066=
NM_001281493.2:c.2681A= (MSH6)	NP_001268422.1:p.Glu894=
NM_001281494.2:c.2681A= (MSH6)	NP_001268423.1:p.Glu894=