Canonical Allele Identifier: CA2496054229

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806350G= , CM000664.2:g.47806350G=	GRCh38
NC_000002.11:g.48033489G= , CM000664.1:g.48033489G=	GRCh37
NC_000002.10:g.47886993G=	NCBI36
NG_007111.1:g.28204G= , LRG_219:g.28204G=
NG_008397.1:g.104326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3496G= (MSH6)	ENSP00000406248.2:p.Gly1166=
ENST00000420813.6:c.3496G= (MSH6)	ENSP00000390382.2:p.Gly1166=
ENST00000455383.6:c.3496G= (MSH6)	ENSP00000397484.2:p.Gly1166=
ENST00000700004.2:c.3409G= (MSH6)	ENSP00000514752.2:p.Gly1137=
ENST00000699999.1:n.4467G= (MSH6)
ENST00000700000.1:c.2227G= (MSH6)	ENSP00000514749.1:p.Gly743=
ENST00000700002.1:c.3799G= (MSH6)	ENSP00000514750.1:p.Gly1267=
ENST00000700003.1:c.1248G= (MSH6)	ENSP00000514751.1:n.1248G=
ENST00000700004.1:c.2566G= (MSH6)	ENSP00000514752.1:p.Gly856=
ENST00000700005.1:n.2644G= (MSH6)
ENST00000700006.1:n.4951G= (MSH6)
ENST00000700007.1:n.2388G= (MSH6)
ENST00000700008.1:n.1962G= (MSH6)
ENST00000700009.1:n.2457G= (MSH6)
ENST00000700010.1:n.1202G= (MSH6)
ENST00000700011.1:n.3087G= (MSH6)
ENST00000682451.1:n.4398C= (FBXO11)
ENST00000684712.1:n.4660C= (FBXO11)
ENST00000234420.11:c.3793G= (MSH6) MANE Select	ENSP00000234420.5:p.Gly1265=
ENST00000540021.6:c.3403G= (MSH6)	ENSP00000446475.1:p.Gly1135=
ENST00000652107.1:c.3496G= (MSH6)	ENSP00000498629.1:p.Gly1166=
ENST00000673637.1:c.3496G= (MSH6)	ENSP00000501310.1:p.Gly1166=
ENST00000234420.9:c.3793G= (MSH6)	ENSP00000234420.4:p.Gly1265=
ENST00000405808.5:c.169+1845C= (FBXO11)	ENSP00000385127.1:n.169+1845C=
ENST00000434234.5:c.*124+1644C= (FBXO11)	ENSP00000402692.1:n.*124+1644C=
ENST00000445503.5:c.*3140G= (MSH6)	ENSP00000405294.1:n.*3140G=
ENST00000538136.1:c.2887G= (MSH6)	ENSP00000438580.1:p.Gly963=
ENST00000540021.5:c.3403G= (MSH6)	ENSP00000446475.1:p.Gly1135=
ENST00000614496.4:c.2887G= (MSH6)	ENSP00000477844.1:p.Gly963=
ENST00000622629.4:c.694G= (MSH6)	ENSP00000482078.1:p.Gly232=
NM_000179.2:c.3793G= , LRG_219t1:c.3793G= (MSH6)	NP_000170.1:p.Gly1265=
NM_001281492.1:c.3403G= (MSH6)	NP_001268421.1:p.Gly1135=
NM_001281493.1:c.2887G= (MSH6)	NP_001268422.1:p.Gly963=
NM_001281494.1:c.2887G= (MSH6)	NP_001268423.1:p.Gly963=
XM_005264271.1:c.3496G= (MSH6)	XP_005264328.1:p.Gly1166=
XM_011532798.1:c.3610G= (MSH6)	XP_011531100.1:p.Gly1204=
XM_011532799.1:c.3496G= (MSH6)	XP_011531101.1:p.Gly1166=
XM_011532800.1:c.3496G= (MSH6)	XP_011531102.1:p.Gly1166=
XM_024452819.1:c.3793G= (MSH6)	XP_024308587.1:p.Gly1265=
XM_024452820.1:c.3610G= (MSH6)	XP_024308588.1:p.Gly1204=
XM_024452821.1:c.3496G= (MSH6)	XP_024308589.1:p.Gly1166=
XM_024452822.1:c.2887G= (MSH6)	XP_024308590.1:p.Gly963=
NM_000179.3:c.3793G= (MSH6) MANE Select	NP_000170.1:p.Gly1265=
NM_001281492.2:c.3403G= (MSH6)	NP_001268421.1:p.Gly1135=
NM_001281493.2:c.2887G= (MSH6)	NP_001268422.1:p.Gly963=
NM_001281494.2:c.2887G= (MSH6)	NP_001268423.1:p.Gly963=