Canonical Allele Identifier: CA2496051919

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803567A= , CM000664.2:g.47803567A=	GRCh38
NC_000002.11:g.48030706A= , CM000664.1:g.48030706A=	GRCh37
NC_000002.10:g.47884210A=	NCBI36
NG_007111.1:g.25421A= , LRG_219:g.25421A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3023A= (MSH6)	ENSP00000406248.2:p.Asp1008=
ENST00000420813.6:c.3023A= (MSH6)	ENSP00000390382.2:p.Asp1008=
ENST00000455383.6:c.3023A= (MSH6)	ENSP00000397484.2:p.Asp1008=
ENST00000700004.2:c.3173-2051A= (MSH6)	ENSP00000514752.2:n.3173-2051A=
ENST00000699999.1:n.3404A= (MSH6)
ENST00000700000.1:c.1754A= (MSH6)	ENSP00000514749.1:p.Asp585=
ENST00000700002.1:c.3326A= (MSH6)	ENSP00000514750.1:p.Asp1109=
ENST00000700003.1:c.775A= (MSH6)	ENSP00000514751.1:n.775A=
ENST00000700004.1:c.2330-2051A= (MSH6)	ENSP00000514752.1:n.2330-2051A=
ENST00000700005.1:n.2171A= (MSH6)
ENST00000700006.1:n.2168A= (MSH6)
ENST00000700007.1:n.1325A= (MSH6)
ENST00000700008.1:n.899A= (MSH6)
ENST00000700009.1:n.898A= (MSH6)
ENST00000700010.1:n.729A= (MSH6)
ENST00000700011.1:n.800A= (MSH6)
ENST00000234420.11:c.3320A= (MSH6) MANE Select	ENSP00000234420.5:p.Asp1107=
ENST00000540021.6:c.2930A= (MSH6)	ENSP00000446475.1:p.Asp977=
ENST00000652107.1:c.3023A= (MSH6)	ENSP00000498629.1:p.Asp1008=
ENST00000673637.1:c.3023A= (MSH6)	ENSP00000501310.1:p.Asp1008=
ENST00000234420.9:c.3320A= (MSH6)	ENSP00000234420.4:p.Asp1107=
ENST00000405808.5:c.169+4628T= (FBXO11)	ENSP00000385127.1:n.169+4628T=
ENST00000434234.5:c.*124+4427T= (FBXO11)	ENSP00000402692.1:n.*124+4427T=
ENST00000445503.5:c.*2667A= (MSH6)	ENSP00000405294.1:n.*2667A=
ENST00000538136.1:c.2414A= (MSH6)	ENSP00000438580.1:p.Asp805=
ENST00000540021.5:c.2930A= (MSH6)	ENSP00000446475.1:p.Asp977=
ENST00000614496.4:c.2414A= (MSH6)	ENSP00000477844.1:p.Asp805=
ENST00000622629.4:c.224A= (MSH6)	ENSP00000482078.1:p.Asp75=
NM_000179.2:c.3320A= , LRG_219t1:c.3320A= (MSH6)	NP_000170.1:p.Asp1107=
NM_001281492.1:c.2930A= (MSH6)	NP_001268421.1:p.Asp977=
NM_001281493.1:c.2414A= (MSH6)	NP_001268422.1:p.Asp805=
NM_001281494.1:c.2414A= (MSH6)	NP_001268423.1:p.Asp805=
XM_005264271.1:c.3023A= (MSH6)	XP_005264328.1:p.Asp1008=
XM_011532798.1:c.3137A= (MSH6)	XP_011531100.1:p.Asp1046=
XM_011532799.1:c.3023A= (MSH6)	XP_011531101.1:p.Asp1008=
XM_011532800.1:c.3023A= (MSH6)	XP_011531102.1:p.Asp1008=
XM_024452819.1:c.3320A= (MSH6)	XP_024308587.1:p.Asp1107=
XM_024452820.1:c.3137A= (MSH6)	XP_024308588.1:p.Asp1046=
XM_024452821.1:c.3023A= (MSH6)	XP_024308589.1:p.Asp1008=
XM_024452822.1:c.2414A= (MSH6)	XP_024308590.1:p.Asp805=
NM_000179.3:c.3320A= (MSH6) MANE Select	NP_000170.1:p.Asp1107=
NM_001281492.2:c.2930A= (MSH6)	NP_001268421.1:p.Asp977=
NM_001281493.2:c.2414A= (MSH6)	NP_001268422.1:p.Asp805=
NM_001281494.2:c.2414A= (MSH6)	NP_001268423.1:p.Asp805=