Canonical Allele Identifier: CA2496054102

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806274A= , CM000664.2:g.47806274A=	GRCh38
NC_000002.11:g.48033413A= , CM000664.1:g.48033413A=	GRCh37
NC_000002.10:g.47886917A=	NCBI36
NG_007111.1:g.28128A= , LRG_219:g.28128A=
NG_008397.1:g.104402T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3420A= (MSH6)	ENSP00000406248.2:p.Ile1140=
ENST00000420813.6:c.3420A= (MSH6)	ENSP00000390382.2:p.Ile1140=
ENST00000455383.6:c.3420A= (MSH6)	ENSP00000397484.2:p.Ile1140=
ENST00000700004.2:c.3333A= (MSH6)	ENSP00000514752.2:p.Ile1111=
ENST00000699999.1:n.4391A= (MSH6)
ENST00000700000.1:c.2151A= (MSH6)	ENSP00000514749.1:p.Ile717=
ENST00000700002.1:c.3723A= (MSH6)	ENSP00000514750.1:p.Ile1241=
ENST00000700003.1:c.1172A= (MSH6)	ENSP00000514751.1:n.1172A=
ENST00000700004.1:c.2490A= (MSH6)	ENSP00000514752.1:p.Ile830=
ENST00000700005.1:n.2568A= (MSH6)
ENST00000700006.1:n.4875A= (MSH6)
ENST00000700007.1:n.2312A= (MSH6)
ENST00000700008.1:n.1886A= (MSH6)
ENST00000700009.1:n.2381A= (MSH6)
ENST00000700010.1:n.1126A= (MSH6)
ENST00000700011.1:n.3011A= (MSH6)
ENST00000682451.1:n.4474T= (FBXO11)
ENST00000684712.1:n.4736T= (FBXO11)
ENST00000234420.11:c.3717A= (MSH6) MANE Select	ENSP00000234420.5:p.Ile1239=
ENST00000540021.6:c.3327A= (MSH6)	ENSP00000446475.1:p.Ile1109=
ENST00000652107.1:c.3420A= (MSH6)	ENSP00000498629.1:p.Ile1140=
ENST00000673637.1:c.3420A= (MSH6)	ENSP00000501310.1:p.Ile1140=
ENST00000234420.9:c.3717A= (MSH6)	ENSP00000234420.4:p.Ile1239=
ENST00000405808.5:c.169+1921T= (FBXO11)	ENSP00000385127.1:n.169+1921T=
ENST00000434234.5:c.*124+1720T= (FBXO11)	ENSP00000402692.1:n.*124+1720T=
ENST00000445503.5:c.*3064A= (MSH6)	ENSP00000405294.1:n.*3064A=
ENST00000538136.1:c.2811A= (MSH6)	ENSP00000438580.1:p.Ile937=
ENST00000540021.5:c.3327A= (MSH6)	ENSP00000446475.1:p.Ile1109=
ENST00000614496.4:c.2811A= (MSH6)	ENSP00000477844.1:p.Ile937=
ENST00000622629.4:c.621A= (MSH6)	ENSP00000482078.1:p.Ile207=
NM_000179.2:c.3717A= , LRG_219t1:c.3717A= (MSH6)	NP_000170.1:p.Ile1239=
NM_001281492.1:c.3327A= (MSH6)	NP_001268421.1:p.Ile1109=
NM_001281493.1:c.2811A= (MSH6)	NP_001268422.1:p.Ile937=
NM_001281494.1:c.2811A= (MSH6)	NP_001268423.1:p.Ile937=
XM_005264271.1:c.3420A= (MSH6)	XP_005264328.1:p.Ile1140=
XM_011532798.1:c.3534A= (MSH6)	XP_011531100.1:p.Ile1178=
XM_011532799.1:c.3420A= (MSH6)	XP_011531101.1:p.Ile1140=
XM_011532800.1:c.3420A= (MSH6)	XP_011531102.1:p.Ile1140=
XM_024452819.1:c.3717A= (MSH6)	XP_024308587.1:p.Ile1239=
XM_024452820.1:c.3534A= (MSH6)	XP_024308588.1:p.Ile1178=
XM_024452821.1:c.3420A= (MSH6)	XP_024308589.1:p.Ile1140=
XM_024452822.1:c.2811A= (MSH6)	XP_024308590.1:p.Ile937=
NM_000179.3:c.3717A= (MSH6) MANE Select	NP_000170.1:p.Ile1239=
NM_001281492.2:c.3327A= (MSH6)	NP_001268421.1:p.Ile1109=
NM_001281493.2:c.2811A= (MSH6)	NP_001268422.1:p.Ile937=
NM_001281494.2:c.2811A= (MSH6)	NP_001268423.1:p.Ile937=