Canonical Allele Identifier: CA2496054551

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806798G= , CM000664.2:g.47806798G=	GRCh38
NC_000002.11:g.48033937G= , CM000664.1:g.48033937G=	GRCh37
NC_000002.10:g.47887441G=	NCBI36
NG_007111.1:g.28652G= , LRG_219:g.28652G=
NG_008397.1:g.103878C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3724G= (MSH6)	ENSP00000406248.2:p.Glu1242=
ENST00000420813.6:c.3724G= (MSH6)	ENSP00000390382.2:p.Glu1242=
ENST00000455383.6:c.3724G= (MSH6)	ENSP00000397484.2:p.Glu1242=
ENST00000700004.2:c.3637G= (MSH6)	ENSP00000514752.2:p.Glu1213=
ENST00000699999.1:n.4695G= (MSH6)
ENST00000700000.1:c.2455G= (MSH6)	ENSP00000514749.1:p.Glu819=
ENST00000700002.1:c.4027G= (MSH6)	ENSP00000514750.1:p.Glu1343=
ENST00000700003.1:c.1476G= (MSH6)	ENSP00000514751.1:n.1476G=
ENST00000700004.1:c.2794G= (MSH6)	ENSP00000514752.1:p.Glu932=
ENST00000700005.1:n.2999G= (MSH6)
ENST00000700007.1:n.2616G= (MSH6)
ENST00000700008.1:n.2283G= (MSH6)
ENST00000700009.1:n.2685G= (MSH6)
ENST00000700010.1:n.1430G= (MSH6)
ENST00000700011.1:n.3315G= (MSH6)
ENST00000682451.1:n.3950C= (FBXO11)
ENST00000684712.1:n.4212C= (FBXO11)
ENST00000234420.11:c.4021G= (MSH6) MANE Select	ENSP00000234420.5:p.Glu1341=
ENST00000540021.6:c.3631G= (MSH6)	ENSP00000446475.1:p.Glu1211=
ENST00000652107.1:c.3724G= (MSH6)	ENSP00000498629.1:p.Glu1242=
ENST00000673637.1:c.3724G= (MSH6)	ENSP00000501310.1:p.Glu1242=
ENST00000234420.9:c.4021G= (MSH6)	ENSP00000234420.4:p.Glu1341=
ENST00000405808.5:c.169+1397C= (FBXO11)	ENSP00000385127.1:n.169+1397C=
ENST00000434234.5:c.*124+1196C= (FBXO11)	ENSP00000402692.1:n.*124+1196C=
ENST00000445503.5:c.*3368G= (MSH6)	ENSP00000405294.1:n.*3368G=
ENST00000465204.5:n.3112C= (FBXO11)
ENST00000538136.1:c.3115G= (MSH6)	ENSP00000438580.1:p.Glu1039=
ENST00000540021.5:c.3631G= (MSH6)	ENSP00000446475.1:p.Glu1211=
ENST00000614496.4:c.3115G= (MSH6)	ENSP00000477844.1:p.Glu1039=
ENST00000622629.4:c.922G= (MSH6)	ENSP00000482078.1:p.Glu308=
NM_000179.2:c.4021G= , LRG_219t1:c.4021G= (MSH6)	NP_000170.1:p.Glu1341=
NM_001281492.1:c.3631G= (MSH6)	NP_001268421.1:p.Glu1211=
NM_001281493.1:c.3115G= (MSH6)	NP_001268422.1:p.Glu1039=
NM_001281494.1:c.3115G= (MSH6)	NP_001268423.1:p.Glu1039=
XM_005264271.1:c.3724G= (MSH6)	XP_005264328.1:p.Glu1242=
XM_011532798.1:c.3838G= (MSH6)	XP_011531100.1:p.Glu1280=
XM_011532799.1:c.3724G= (MSH6)	XP_011531101.1:p.Glu1242=
XM_011532800.1:c.3724G= (MSH6)	XP_011531102.1:p.Glu1242=
XM_024452819.1:c.4114G= (MSH6)	XP_024308587.1:p.Glu1372=
XM_024452820.1:c.3931G= (MSH6)	XP_024308588.1:p.Glu1311=
XM_024452821.1:c.3817G= (MSH6)	XP_024308589.1:p.Glu1273=
XM_024452822.1:c.3208G= (MSH6)	XP_024308590.1:p.Glu1070=
NM_000179.3:c.4021G= (MSH6) MANE Select	NP_000170.1:p.Glu1341=
NM_001281492.2:c.3631G= (MSH6)	NP_001268421.1:p.Glu1211=
NM_001281493.2:c.3115G= (MSH6)	NP_001268422.1:p.Glu1039=
NM_001281494.2:c.3115G= (MSH6)	NP_001268423.1:p.Glu1039=