Canonical Allele Identifier: CA2496054004

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806216C= , CM000664.2:g.47806216C=	GRCh38
NC_000002.11:g.48033355C= , CM000664.1:g.48033355C=	GRCh37
NC_000002.10:g.47886859C=	NCBI36
NG_007111.1:g.28070C= , LRG_219:g.28070C=
NG_008397.1:g.104460G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3362C= (MSH6)	ENSP00000406248.2:p.Ala1121=
ENST00000420813.6:c.3362C= (MSH6)	ENSP00000390382.2:p.Ala1121=
ENST00000455383.6:c.3362C= (MSH6)	ENSP00000397484.2:p.Ala1121=
ENST00000700004.2:c.3275C= (MSH6)	ENSP00000514752.2:p.Ala1092=
ENST00000699999.1:n.4333C= (MSH6)
ENST00000700000.1:c.2093C= (MSH6)	ENSP00000514749.1:p.Ala698=
ENST00000700002.1:c.3665C= (MSH6)	ENSP00000514750.1:p.Ala1222=
ENST00000700003.1:c.1114C= (MSH6)	ENSP00000514751.1:n.1114C=
ENST00000700004.1:c.2432C= (MSH6)	ENSP00000514752.1:p.Ala811=
ENST00000700005.1:n.2510C= (MSH6)
ENST00000700006.1:n.4817C= (MSH6)
ENST00000700007.1:n.2254C= (MSH6)
ENST00000700008.1:n.1828C= (MSH6)
ENST00000700009.1:n.2323C= (MSH6)
ENST00000700010.1:n.1068C= (MSH6)
ENST00000700011.1:n.2953C= (MSH6)
ENST00000682451.1:n.4532G= (FBXO11)
ENST00000684712.1:n.4794G= (FBXO11)
ENST00000234420.11:c.3659C= (MSH6) MANE Select	ENSP00000234420.5:p.Ala1220=
ENST00000540021.6:c.3269C= (MSH6)	ENSP00000446475.1:p.Ala1090=
ENST00000652107.1:c.3362C= (MSH6)	ENSP00000498629.1:p.Ala1121=
ENST00000673637.1:c.3362C= (MSH6)	ENSP00000501310.1:p.Ala1121=
ENST00000234420.9:c.3659C= (MSH6)	ENSP00000234420.4:p.Ala1220=
ENST00000405808.5:c.169+1979G= (FBXO11)	ENSP00000385127.1:n.169+1979G=
ENST00000434234.5:c.*124+1778G= (FBXO11)	ENSP00000402692.1:n.*124+1778G=
ENST00000445503.5:c.*3006C= (MSH6)	ENSP00000405294.1:n.*3006C=
ENST00000538136.1:c.2753C= (MSH6)	ENSP00000438580.1:p.Ala918=
ENST00000540021.5:c.3269C= (MSH6)	ENSP00000446475.1:p.Ala1090=
ENST00000614496.4:c.2753C= (MSH6)	ENSP00000477844.1:p.Ala918=
ENST00000622629.4:c.563C= (MSH6)	ENSP00000482078.1:p.Ala188=
NM_000179.2:c.3659C= , LRG_219t1:c.3659C= (MSH6)	NP_000170.1:p.Ala1220=
NM_001281492.1:c.3269C= (MSH6)	NP_001268421.1:p.Ala1090=
NM_001281493.1:c.2753C= (MSH6)	NP_001268422.1:p.Ala918=
NM_001281494.1:c.2753C= (MSH6)	NP_001268423.1:p.Ala918=
XM_005264271.1:c.3362C= (MSH6)	XP_005264328.1:p.Ala1121=
XM_011532798.1:c.3476C= (MSH6)	XP_011531100.1:p.Ala1159=
XM_011532799.1:c.3362C= (MSH6)	XP_011531101.1:p.Ala1121=
XM_011532800.1:c.3362C= (MSH6)	XP_011531102.1:p.Ala1121=
XM_024452819.1:c.3659C= (MSH6)	XP_024308587.1:p.Ala1220=
XM_024452820.1:c.3476C= (MSH6)	XP_024308588.1:p.Ala1159=
XM_024452821.1:c.3362C= (MSH6)	XP_024308589.1:p.Ala1121=
XM_024452822.1:c.2753C= (MSH6)	XP_024308590.1:p.Ala918=
NM_000179.3:c.3659C= (MSH6) MANE Select	NP_000170.1:p.Ala1220=
NM_001281492.2:c.3269C= (MSH6)	NP_001268421.1:p.Ala1090=
NM_001281493.2:c.2753C= (MSH6)	NP_001268422.1:p.Ala918=
NM_001281494.2:c.2753C= (MSH6)	NP_001268423.1:p.Ala918=