Canonical Allele Identifier: CA2496054348

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806625G= , CM000664.2:g.47806625G=	GRCh38
NC_000002.11:g.48033764G= , CM000664.1:g.48033764G=	GRCh37
NC_000002.10:g.47887268G=	NCBI36
NG_007111.1:g.28479G= , LRG_219:g.28479G=
NG_008397.1:g.104051C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3678G= (MSH6)	ENSP00000406248.2:p.Lys1226=
ENST00000420813.6:c.3678G= (MSH6)	ENSP00000390382.2:p.Lys1226=
ENST00000455383.6:c.3678G= (MSH6)	ENSP00000397484.2:p.Lys1226=
ENST00000700004.2:c.3591G= (MSH6)	ENSP00000514752.2:p.Lys1197=
ENST00000699999.1:n.4649G= (MSH6)
ENST00000700000.1:c.2409G= (MSH6)	ENSP00000514749.1:p.Lys803=
ENST00000700002.1:c.3981G= (MSH6)	ENSP00000514750.1:p.Lys1327=
ENST00000700003.1:c.1430G= (MSH6)	ENSP00000514751.1:n.1430G=
ENST00000700004.1:c.2748G= (MSH6)	ENSP00000514752.1:p.Lys916=
ENST00000700005.1:n.2826G= (MSH6)
ENST00000700006.1:n.5133G= (MSH6)
ENST00000700007.1:n.2570G= (MSH6)
ENST00000700008.1:n.2237G= (MSH6)
ENST00000700009.1:n.2639G= (MSH6)
ENST00000700010.1:n.1384G= (MSH6)
ENST00000700011.1:n.3269G= (MSH6)
ENST00000682451.1:n.4123C= (FBXO11)
ENST00000684712.1:n.4385C= (FBXO11)
ENST00000234420.11:c.3975G= (MSH6) MANE Select	ENSP00000234420.5:p.Lys1325=
ENST00000540021.6:c.3585G= (MSH6)	ENSP00000446475.1:p.Lys1195=
ENST00000652107.1:c.3678G= (MSH6)	ENSP00000498629.1:p.Lys1226=
ENST00000673637.1:c.3678G= (MSH6)	ENSP00000501310.1:p.Lys1226=
ENST00000234420.9:c.3975G= (MSH6)	ENSP00000234420.4:p.Lys1325=
ENST00000405808.5:c.169+1570C= (FBXO11)	ENSP00000385127.1:n.169+1570C=
ENST00000434234.5:c.*124+1369C= (FBXO11)	ENSP00000402692.1:n.*124+1369C=
ENST00000445503.5:c.*3322G= (MSH6)	ENSP00000405294.1:n.*3322G=
ENST00000538136.1:c.3069G= (MSH6)	ENSP00000438580.1:p.Lys1023=
ENST00000540021.5:c.3585G= (MSH6)	ENSP00000446475.1:p.Lys1195=
ENST00000614496.4:c.3069G= (MSH6)	ENSP00000477844.1:p.Lys1023=
ENST00000622629.4:c.876G= (MSH6)	ENSP00000482078.1:p.Lys292=
NM_000179.2:c.3975G= , LRG_219t1:c.3975G= (MSH6)	NP_000170.1:p.Lys1325=
NM_001281492.1:c.3585G= (MSH6)	NP_001268421.1:p.Lys1195=
NM_001281493.1:c.3069G= (MSH6)	NP_001268422.1:p.Lys1023=
NM_001281494.1:c.3069G= (MSH6)	NP_001268423.1:p.Lys1023=
XM_005264271.1:c.3678G= (MSH6)	XP_005264328.1:p.Lys1226=
XM_011532798.1:c.3792G= (MSH6)	XP_011531100.1:p.Lys1264=
XM_011532799.1:c.3678G= (MSH6)	XP_011531101.1:p.Lys1226=
XM_011532800.1:c.3678G= (MSH6)	XP_011531102.1:p.Lys1226=
XM_024452819.1:c.4068G= (MSH6)	XP_024308587.1:p.Lys1356=
XM_024452820.1:c.3885G= (MSH6)	XP_024308588.1:p.Lys1295=
XM_024452821.1:c.3771G= (MSH6)	XP_024308589.1:p.Lys1257=
XM_024452822.1:c.3162G= (MSH6)	XP_024308590.1:p.Lys1054=
NM_000179.3:c.3975G= (MSH6) MANE Select	NP_000170.1:p.Lys1325=
NM_001281492.2:c.3585G= (MSH6)	NP_001268421.1:p.Lys1195=
NM_001281493.2:c.3069G= (MSH6)	NP_001268422.1:p.Lys1023=
NM_001281494.2:c.3069G= (MSH6)	NP_001268423.1:p.Lys1023=