Canonical Allele Identifier: CA2830782454

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799504_47799505del , CM000664.2:g.47799504_47799505del	GRCh38
NC_000002.11:g.48026643_48026644del , CM000664.1:g.48026643_48026644del	GRCh37
NC_000002.10:g.47880147_47880148del	NCBI36
NG_007111.1:g.21358_21359del , LRG_219:g.21358_21359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1224_1225del (MSH6)	ENSP00000406248.2:p.Arg408SerfsTer8
ENST00000420813.6:c.1224_1225del (MSH6)	ENSP00000390382.2:p.Arg408SerfsTer8
ENST00000455383.6:c.1224_1225del (MSH6)	ENSP00000397484.2:p.Arg408SerfsTer8
ENST00000700004.2:c.1521_1522del (MSH6)	ENSP00000514752.2:p.Arg507SerfsTer8
ENST00000699999.1:n.1605_1606del (MSH6)
ENST00000700000.1:c.1521_1522del (MSH6)	ENSP00000514749.1:p.Arg507SerfsTer8
ENST00000700002.1:c.1527_1528del (MSH6)	ENSP00000514750.1:p.Arg509SerfsTer8
ENST00000700003.1:c.627+3441_627+3442del (MSH6)	ENSP00000514751.1:n.627+3441_627+3442del
ENST00000700004.1:c.678_679del (MSH6)	ENSP00000514752.1:p.Arg226SerfsTer8
ENST00000234420.11:c.1521_1522del (MSH6) MANE Select	ENSP00000234420.5:p.Arg507SerfsTer8
ENST00000540021.6:c.1131_1132del (MSH6)	ENSP00000446475.1:p.Arg377SerfsTer8
ENST00000652107.1:c.1224_1225del (MSH6)	ENSP00000498629.1:p.Arg408SerfsTer8
ENST00000673637.1:c.1224_1225del (MSH6)	ENSP00000501310.1:p.Arg408SerfsTer8
ENST00000234420.9:c.1521_1522del (MSH6)	ENSP00000234420.4:p.Arg507SerfsTer8
ENST00000405808.5:c.169+8692_169+8693del (FBXO11)	ENSP00000385127.1:n.169+8692_169+8693del
ENST00000434234.5:c.*124+8491_*124+8492del (FBXO11)	ENSP00000402692.1:n.*124+8491_*124+8492del
ENST00000445503.5:c.*868_*869del (MSH6)	ENSP00000405294.1:n.*868_*869del
ENST00000538136.1:c.615_616del (MSH6)	ENSP00000438580.1:p.Arg205SerfsTer8
ENST00000540021.5:c.1131_1132del (MSH6)	ENSP00000446475.1:p.Arg377SerfsTer8
ENST00000614496.4:c.615_616del (MSH6)	ENSP00000477844.1:p.Arg205SerfsTer8
ENST00000616033.4:c.1518_1519del (MSH6)	ENSP00000480261.1:p.Arg506SerfsTer8
ENST00000622629.4:c.-1576_-1575del (MSH6)	ENSP00000482078.1:n.-1576_-1575del
NM_000179.2:c.1521_1522del , LRG_219t1:c.1521_1522del (MSH6)	NP_000170.1:p.Arg507SerfsTer8
NM_001281492.1:c.1131_1132del (MSH6)	NP_001268421.1:p.Arg377SerfsTer8
NM_001281493.1:c.615_616del (MSH6)	NP_001268422.1:p.Arg205SerfsTer8
NM_001281494.1:c.615_616del (MSH6)	NP_001268423.1:p.Arg205SerfsTer8
XM_005264271.1:c.1224_1225del (MSH6)	XP_005264328.1:p.Arg408SerfsTer8
XM_011532798.1:c.1338_1339del (MSH6)	XP_011531100.1:p.Arg446SerfsTer8
XM_011532799.1:c.1224_1225del (MSH6)	XP_011531101.1:p.Arg408SerfsTer8
XM_011532800.1:c.1224_1225del (MSH6)	XP_011531102.1:p.Arg408SerfsTer8
XM_024452819.1:c.1521_1522del (MSH6)	XP_024308587.1:p.Arg507SerfsTer8
XM_024452820.1:c.1338_1339del (MSH6)	XP_024308588.1:p.Arg446SerfsTer8
XM_024452821.1:c.1224_1225del (MSH6)	XP_024308589.1:p.Arg408SerfsTer8
XM_024452822.1:c.615_616del (MSH6)	XP_024308590.1:p.Arg205SerfsTer8
NM_000179.3:c.1521_1522del (MSH6) MANE Select	NP_000170.1:p.Arg507SerfsTer8
NM_001281492.2:c.1131_1132del (MSH6)	NP_001268421.1:p.Arg377SerfsTer8
NM_001281493.2:c.615_616del (MSH6)	NP_001268422.1:p.Arg205SerfsTer8
NM_001281494.2:c.615_616del (MSH6)	NP_001268423.1:p.Arg205SerfsTer8