Canonical Allele Identifier: CA2573130185

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1433761
• ClinVar RCV Id: RCV001952718 ; RCV002344079 ; RCV003447608
• dbSNP Id: rs2104541388

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806277dup , CM000664.2:g.47806277dup	GRCh38
NC_000002.11:g.48033416dup , CM000664.1:g.48033416dup	GRCh37
NC_000002.10:g.47886920dup	NCBI36
NG_007111.1:g.28131dup , LRG_219:g.28131dup
NG_008397.1:g.104402dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3423dup (MSH6)	ENSP00000406248.2:p.Cys1142MetfsTer?
ENST00000420813.6:c.3423dup (MSH6)	ENSP00000390382.2:p.Cys1142MetfsTer?
ENST00000455383.6:c.3423dup (MSH6)	ENSP00000397484.2:p.Cys1142MetfsTer?
ENST00000700004.2:c.3336dup (MSH6)	ENSP00000514752.2:p.Cys1113MetfsTer?
ENST00000699999.1:n.4394dup (MSH6)
ENST00000700000.1:c.2154dup (MSH6)	ENSP00000514749.1:p.Cys719MetfsTer?
ENST00000700002.1:c.3726dup (MSH6)	ENSP00000514750.1:p.Cys1243MetfsTer?
ENST00000700003.1:c.1175dup (MSH6)	ENSP00000514751.1:n.1175dup
ENST00000700004.1:c.2493dup (MSH6)	ENSP00000514752.1:p.Cys832MetfsTer?
ENST00000700005.1:n.2571dup (MSH6)
ENST00000700006.1:n.4878dup (MSH6)
ENST00000700007.1:n.2315dup (MSH6)
ENST00000700008.1:n.1889dup (MSH6)
ENST00000700009.1:n.2384dup (MSH6)
ENST00000700010.1:n.1129dup (MSH6)
ENST00000700011.1:n.3014dup (MSH6)
ENST00000682451.1:n.4474dup (FBXO11)
ENST00000684712.1:n.4736dup (FBXO11)
ENST00000234420.11:c.3720dup (MSH6) MANE Select	ENSP00000234420.5:p.Cys1241MetfsTer?
ENST00000540021.6:c.3330dup (MSH6)	ENSP00000446475.1:p.Cys1111MetfsTer?
ENST00000652107.1:c.3423dup (MSH6)	ENSP00000498629.1:p.Cys1142MetfsTer?
ENST00000673637.1:c.3423dup (MSH6)	ENSP00000501310.1:p.Cys1142MetfsTer?
ENST00000234420.9:c.3720dup (MSH6)	ENSP00000234420.4:p.Cys1241MetfsTer?
ENST00000405808.5:c.169+1921dup (FBXO11)	ENSP00000385127.1:n.169+1921dup
ENST00000434234.5:c.*124+1720dup (FBXO11)	ENSP00000402692.1:n.*124+1720dup
ENST00000445503.5:c.*3067dup (MSH6)	ENSP00000405294.1:n.*3067dup
ENST00000538136.1:c.2814dup (MSH6)	ENSP00000438580.1:p.Cys939MetfsTer?
ENST00000540021.5:c.3330dup (MSH6)	ENSP00000446475.1:p.Cys1111MetfsTer?
ENST00000614496.4:c.2814dup (MSH6)	ENSP00000477844.1:p.Cys939MetfsTer?
ENST00000622629.4:c.624dup (MSH6)	ENSP00000482078.1:p.Cys209MetfsTer12
NM_000179.2:c.3720dup , LRG_219t1:c.3720dup (MSH6)	NP_000170.1:p.Cys1241MetfsTer?
NM_001281492.1:c.3330dup (MSH6)	NP_001268421.1:p.Cys1111MetfsTer?
NM_001281493.1:c.2814dup (MSH6)	NP_001268422.1:p.Cys939MetfsTer?
NM_001281494.1:c.2814dup (MSH6)	NP_001268423.1:p.Cys939MetfsTer?
XM_005264271.1:c.3423dup (MSH6)	XP_005264328.1:p.Cys1142MetfsTer?
XM_011532798.1:c.3537dup (MSH6)	XP_011531100.1:p.Cys1180MetfsTer?
XM_011532799.1:c.3423dup (MSH6)	XP_011531101.1:p.Cys1142MetfsTer?
XM_011532800.1:c.3423dup (MSH6)	XP_011531102.1:p.Cys1142MetfsTer?
XM_024452819.1:c.3720dup (MSH6)	XP_024308587.1:p.Cys1241MetfsTer?
XM_024452820.1:c.3537dup (MSH6)	XP_024308588.1:p.Cys1180MetfsTer?
XM_024452821.1:c.3423dup (MSH6)	XP_024308589.1:p.Cys1142MetfsTer?
XM_024452822.1:c.2814dup (MSH6)	XP_024308590.1:p.Cys939MetfsTer?
NM_000179.3:c.3720dup (MSH6) MANE Select	NP_000170.1:p.Cys1241MetfsTer?
NM_001281492.2:c.3330dup (MSH6)	NP_001268421.1:p.Cys1111MetfsTer?
NM_001281493.2:c.2814dup (MSH6)	NP_001268422.1:p.Cys939MetfsTer?
NM_001281494.2:c.2814dup (MSH6)	NP_001268423.1:p.Cys939MetfsTer?