Canonical Allele Identifier: CA2739274375

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2853558
• ClinVar RCV Id: RCV003758669

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806240del , CM000664.2:g.47806240del	GRCh38
NC_000002.11:g.48033379del , CM000664.1:g.48033379del	GRCh37
NC_000002.10:g.47886883del	NCBI36
NG_007111.1:g.28094del , LRG_219:g.28094del
NG_008397.1:g.104436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3386del (MSH6)	ENSP00000406248.2:p.Ala1129GlufsTer12
ENST00000420813.6:c.3386del (MSH6)	ENSP00000390382.2:p.Ala1129GlufsTer12
ENST00000455383.6:c.3386del (MSH6)	ENSP00000397484.2:p.Ala1129GlufsTer12
ENST00000700004.2:c.3299del (MSH6)	ENSP00000514752.2:p.Ala1100GlufsTer12
ENST00000699999.1:n.4357del (MSH6)
ENST00000700000.1:c.2117del (MSH6)	ENSP00000514749.1:p.Ala706GlufsTer12
ENST00000700002.1:c.3689del (MSH6)	ENSP00000514750.1:p.Ala1230GlufsTer12
ENST00000700003.1:c.1138del (MSH6)	ENSP00000514751.1:n.1138del
ENST00000700004.1:c.2456del (MSH6)	ENSP00000514752.1:p.Ala819GlufsTer12
ENST00000700005.1:n.2534del (MSH6)
ENST00000700006.1:n.4841del (MSH6)
ENST00000700007.1:n.2278del (MSH6)
ENST00000700008.1:n.1852del (MSH6)
ENST00000700009.1:n.2347del (MSH6)
ENST00000700010.1:n.1092del (MSH6)
ENST00000700011.1:n.2977del (MSH6)
ENST00000682451.1:n.4508del (FBXO11)
ENST00000684712.1:n.4770del (FBXO11)
ENST00000234420.11:c.3683del (MSH6) MANE Select	ENSP00000234420.5:p.Ala1228GlufsTer12
ENST00000540021.6:c.3293del (MSH6)	ENSP00000446475.1:p.Ala1098GlufsTer12
ENST00000652107.1:c.3386del (MSH6)	ENSP00000498629.1:p.Ala1129GlufsTer12
ENST00000673637.1:c.3386del (MSH6)	ENSP00000501310.1:p.Ala1129GlufsTer12
ENST00000234420.9:c.3683del (MSH6)	ENSP00000234420.4:p.Ala1228GlufsTer12
ENST00000405808.5:c.169+1955del (FBXO11)	ENSP00000385127.1:n.169+1955del
ENST00000434234.5:c.*124+1754del (FBXO11)	ENSP00000402692.1:n.*124+1754del
ENST00000445503.5:c.*3030del (MSH6)	ENSP00000405294.1:n.*3030del
ENST00000538136.1:c.2777del (MSH6)	ENSP00000438580.1:p.Ala926GlufsTer12
ENST00000540021.5:c.3293del (MSH6)	ENSP00000446475.1:p.Ala1098GlufsTer12
ENST00000614496.4:c.2777del (MSH6)	ENSP00000477844.1:p.Ala926GlufsTer12
ENST00000622629.4:c.587del (MSH6)	ENSP00000482078.1:p.Ala196GlufsTer12
NM_000179.2:c.3683del , LRG_219t1:c.3683del (MSH6)	NP_000170.1:p.Ala1228GlufsTer12
NM_001281492.1:c.3293del (MSH6)	NP_001268421.1:p.Ala1098GlufsTer12
NM_001281493.1:c.2777del (MSH6)	NP_001268422.1:p.Ala926GlufsTer12
NM_001281494.1:c.2777del (MSH6)	NP_001268423.1:p.Ala926GlufsTer12
XM_005264271.1:c.3386del (MSH6)	XP_005264328.1:p.Ala1129GlufsTer12
XM_011532798.1:c.3500del (MSH6)	XP_011531100.1:p.Ala1167GlufsTer12
XM_011532799.1:c.3386del (MSH6)	XP_011531101.1:p.Ala1129GlufsTer12
XM_011532800.1:c.3386del (MSH6)	XP_011531102.1:p.Ala1129GlufsTer12
XM_024452819.1:c.3683del (MSH6)	XP_024308587.1:p.Ala1228GlufsTer12
XM_024452820.1:c.3500del (MSH6)	XP_024308588.1:p.Ala1167GlufsTer12
XM_024452821.1:c.3386del (MSH6)	XP_024308589.1:p.Ala1129GlufsTer12
XM_024452822.1:c.2777del (MSH6)	XP_024308590.1:p.Ala926GlufsTer12
NM_000179.3:c.3683del (MSH6) MANE Select	NP_000170.1:p.Ala1228GlufsTer12
NM_001281492.2:c.3293del (MSH6)	NP_001268421.1:p.Ala1098GlufsTer12
NM_001281493.2:c.2777del (MSH6)	NP_001268422.1:p.Ala926GlufsTer12
NM_001281494.2:c.2777del (MSH6)	NP_001268423.1:p.Ala926GlufsTer12