Canonical Allele Identifier: CA2580067751

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1785177
• ClinVar RCV Id: RCV002421926 ; RCV003465750 ; RCV003759708

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800042dup , CM000664.2:g.47800042dup	GRCh38
NC_000002.11:g.48027181dup , CM000664.1:g.48027181dup	GRCh37
NC_000002.10:g.47880685dup	NCBI36
NG_007111.1:g.21896dup , LRG_219:g.21896dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1762dup (MSH6)	ENSP00000406248.2:p.Cys588LeufsTer11
ENST00000420813.6:c.1762dup (MSH6)	ENSP00000390382.2:p.Cys588LeufsTer11
ENST00000455383.6:c.1762dup (MSH6)	ENSP00000397484.2:p.Cys588LeufsTer11
ENST00000700004.2:c.2059dup (MSH6)	ENSP00000514752.2:p.Cys687LeufsTer11
ENST00000699999.1:n.2143dup (MSH6)
ENST00000700000.1:c.1606+453dup (MSH6)	ENSP00000514749.1:n.1606+453dup
ENST00000700002.1:c.2065dup (MSH6)	ENSP00000514750.1:p.Cys689LeufsTer11
ENST00000700003.1:c.628-3378dup (MSH6)	ENSP00000514751.1:n.628-3378dup
ENST00000700004.1:c.1216dup (MSH6)	ENSP00000514752.1:p.Cys406LeufsTer11
ENST00000234420.11:c.2059dup (MSH6) MANE Select	ENSP00000234420.5:p.Cys687LeufsTer11
ENST00000540021.6:c.1669dup (MSH6)	ENSP00000446475.1:p.Cys557LeufsTer11
ENST00000652107.1:c.1762dup (MSH6)	ENSP00000498629.1:p.Cys588LeufsTer11
ENST00000673637.1:c.1762dup (MSH6)	ENSP00000501310.1:p.Cys588LeufsTer11
ENST00000234420.9:c.2059dup (MSH6)	ENSP00000234420.4:p.Cys687LeufsTer11
ENST00000405808.5:c.169+8154dup (FBXO11)	ENSP00000385127.1:n.169+8154dup
ENST00000434234.5:c.*124+7953dup (FBXO11)	ENSP00000402692.1:n.*124+7953dup
ENST00000445503.5:c.*1406dup (MSH6)	ENSP00000405294.1:n.*1406dup
ENST00000538136.1:c.1153dup (MSH6)	ENSP00000438580.1:p.Cys385LeufsTer11
ENST00000540021.5:c.1669dup (MSH6)	ENSP00000446475.1:p.Cys557LeufsTer11
ENST00000614496.4:c.1153dup (MSH6)	ENSP00000477844.1:p.Cys385LeufsTer11
ENST00000616033.4:c.2056dup (MSH6)	ENSP00000480261.1:p.Cys686LeufsTer11
ENST00000622629.4:c.-1038dup (MSH6)	ENSP00000482078.1:n.-1038dup
NM_000179.2:c.2059dup , LRG_219t1:c.2059dup (MSH6)	NP_000170.1:p.Cys687LeufsTer11
NM_001281492.1:c.1669dup (MSH6)	NP_001268421.1:p.Cys557LeufsTer11
NM_001281493.1:c.1153dup (MSH6)	NP_001268422.1:p.Cys385LeufsTer11
NM_001281494.1:c.1153dup (MSH6)	NP_001268423.1:p.Cys385LeufsTer11
XM_005264271.1:c.1762dup (MSH6)	XP_005264328.1:p.Cys588LeufsTer11
XM_011532798.1:c.1876dup (MSH6)	XP_011531100.1:p.Cys626LeufsTer11
XM_011532799.1:c.1762dup (MSH6)	XP_011531101.1:p.Cys588LeufsTer11
XM_011532800.1:c.1762dup (MSH6)	XP_011531102.1:p.Cys588LeufsTer11
XM_024452819.1:c.2059dup (MSH6)	XP_024308587.1:p.Cys687LeufsTer11
XM_024452820.1:c.1876dup (MSH6)	XP_024308588.1:p.Cys626LeufsTer11
XM_024452821.1:c.1762dup (MSH6)	XP_024308589.1:p.Cys588LeufsTer11
XM_024452822.1:c.1153dup (MSH6)	XP_024308590.1:p.Cys385LeufsTer11
NM_000179.3:c.2059dup (MSH6) MANE Select	NP_000170.1:p.Cys687LeufsTer11
NM_001281492.2:c.1669dup (MSH6)	NP_001268421.1:p.Cys557LeufsTer11
NM_001281493.2:c.1153dup (MSH6)	NP_001268422.1:p.Cys385LeufsTer11
NM_001281494.2:c.1153dup (MSH6)	NP_001268423.1:p.Cys385LeufsTer11